Methods of Treating Cytokine Mediated Diseases

ABSTRACT

Disclosed are methods of treating acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet&#39;s disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, sepsis, chronic obstructive pulmonary disease, traumatic arthritis, congestive heart failure and restenosis following percutaneous transluminal coronary angioplasty, known to be cytokine mediated, using aromatic heterocyclic compounds described in WO 00/55139.

APPLICATION DATA

This application is a divisional application of U.S. Ser. No. 10/237,306 filed Sep. 9, 2002 which claims benefit to U.S. provisional application Ser. No. 60/318,958 filed Sep. 13, 2001, the entirety of each is incorporated herein by reference.

TECHNICAL FIELD OF THE INVENTION

This invention relates to methods of treating acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure indicated to be cytokine mediated diseases using aromatic heterocyclic compounds disclosed in PCT publication WO 00/55139.

BACKGROUND OF THE INVENTION

In WO 00/55139 there are described aromatic heterocyclic compounds useful in treating certain cytokine mediated diseases. Tumor necrosis factor (TNF) and interleukin-1 (IL-1) are important biological entities collectively referred to as proinflammatory cytokines. These, along with several other related molecules, mediate the inflammatory response associated with the immunological recognition of infectious agents. The inflammatory response plays an important role in limiting and controlling pathogenic infections.

Elevated levels of proinflammatory cytokines are also associated with a number of diseases of autoimmunity such as toxic shock syndrome, rheumatoid arthritis, osteoarthritis, diabetes and inflammatory bowel disease (Dinarello, C. A., et al., 1984, Rev. Infect. Disease 6:51). In these diseases, chronic elevation of inflammation exacerbates or causes much of the pathophysiology observed. For example, rheumatoid synovial tissue becomes invaded with inflammatory cells that result in destruction to cartilage and bone (Koch, A. E., et al., 1995, J. Invest. Med. 43: 28-38). Studies suggest that inflammatory changes mediated by cytokines may be involved in the pathogenesis of restenosis after percutaneous transluminal coronary angioplasty (PTCA) (Tashiro, H., et al., 2001 Mar, Coron Artery Dis 12(2):107-13). An important and accepted therapeutic approach for potential drug intervention in these diseases is the reduction of proinflammatory cytokines such as TNF (also referred to in its secreted cell-free form as TNFα) and IL-1β. A number of anti-cytokine therapies are currently in clinical trials. Efficacy has been demonstrated with a monoclonal antibody directed against TNFα in a number of autoimmune diseases (Heath, P., “CDP571: An Engineered Human IgG4 Anti-TNFα Antibody” IBC Meeting on Cytokine Antagonists, Philadelphia, Pa., Apr. 24-5, 1997). These include the treatment of rheumatoid arthritis, Crohn's disease and ulcerative colitis (Rankin, E. C. C., et al., 1997, British J. Rheum. 35: 334-342 and Stack, W. A., et al., 1997, Lancet 349: 521-524). The monoclonal antibody is thought to function by binding to both soluble TNFα and to membrane bound TNF.

A soluble TNFα receptor has been engineered that interacts with TNFα. The approach is similar to that described above for the monoclonal antibodies directed against TNFα; both agents bind to soluble TNFα, thus reducing its concentration. One version of this construct, called Enbrel (Immunex, Seattle, Wash.) recently demonstrated efficacy in a Phase III clinical trial for the treatment of rheumatoid arthritis (Brower et al., 1997, Nature Biotechnology 15: 1240). Another version of the TNFα receptor, Ro 45-2081 (Hoffman-LaRoche Inc., Nutley, N.J.) has demonstrated efficacy in various animal models of allergic lung inflammation and acute lung injury. Ro 45-2081 is a recombinant chimeric molecule constructed from the soluble 55 kDa human TNF receptor fused to the hinge region of the heavy chain IgG1 gene and expressed in eukaryotic cells (Renzetti, et al., 1997, Inflamm. Res. 46: S143).

IL-1 has been implicated as an immunological effector molecule in a large number of disease processes. IL-1 receptor antagonist (IL-1ra) had been examined in human clinical trials. Efficacy has been demonstrated for the treatment of rheumatoid arthritis (Antril, Amgen). In a phase III human clinical trial IL-1ra reduced the mortality rate in patients with septic shock syndrome (Dinarello, 1995, Nutrution 11, 492). Osteoarthritis is a slow progressive disease characterized by destruction of the articular cartilage. IL-1 is detected in synovial fluid and in the cartilage matrix of osteoarthritic joints. Antagonists of IL-1 have been shown to diminish the degradation of cartilage matrix components in a variety of experimental models of arthritis (Chevalier, 1997, Biomed Pharmacother. 51, 58). Nitric oxide (NO) is a mediator of cardiovascular homeostasis, neurotransmission and immune function; recently it has been shown to have important effects in the modulation of bone remodeling. Cytokines such as IL-1 and TNF are potent stimulators of NO production. NO is an important regulatory molecule in bone with effects on cells of the osteoblast and osteoclast lineage (Evans, et al, 1996, J Bone Miner Res. 11, 300). The promotion of beta-cell destruction leading to insulin dependent diabetes mellitus shows dependence on IL-1. Some of this damage may be mediated through other effectors such as prostaglandins and thromboxanes. IL-1 can effect this process by controlling the level of both cyclooxygenase II and inducible nitric oxide synthetase expression (McDaniel et al., 1996, Proc Soc Exp Biol Med. 211, 24).

Inhibitors of cytokine production are expected to block inducible cyclooxygenase (COX-2) expression. COX-2 expression has been shown to be increased by cytokines and it is believed to be the isoform of cyclooxygenase responsible for inflammation (M. K. O'Banion et al., Proc. Natl. Acad. Sci. U.S.A, 1992, 89, 4888.) Accordingly, inhibitors of cytokines such as IL-1 would be expected to exhibit efficacy against those disorders currently treated with COX inhibitors such as the familiar NSAIDs. These disorders include acute and chronic pain as well as symptoms of inflammation and cardiovascular disease.

Elevation of several cytokines have been demonstrated during active inflammatory bowel disease (IBD). A mucosal imbalance of intestinal IL-1 and IL-1ra is present in patients with IBD. Insufficient production of endogenous IL-1ra may contribute to the pathogenesis of IBD (Cominelli, et al., 1996, Aliment Pharmacol Ther. 10, 49).

Alzheimer disease is characterized by the presence of beta-amyloid protein deposits, neurofibrillary tangles and cholinergic dysfunction throughout the hippocampal region. The structural and metabolic damage found in Alzheimer disease is possibly due to a sustained elevation of IL-1 (Holden, et al., 1995, Med Hypotheses, 45, 559). A role for IL-1 in the pathogenesis of human immunodeficiency virus (HIV) has been identified. IL-1ra showed a clear relationship to acute inflammatory events as well as to the different disease stages in the pathophysiology of HIV infection (Kreuzer, et al., 1997, Clin Exp Immunol. 109, 54). IL-1 and TNF are both involved in periodontal disease. The destructive process associated with periodontal disease may be due to a disregulation of both IL-1 and TNF (Howells, 1995, Oral Dis. 1, 266).

Proinflammatory cytokines such as TNFα and IL-1β are also important mediators of septic shock and associated cardiopulmonary dysfunction, acute respiratory distress syndrome (ARDS) and multiple organ failure. In a study of patients presenting at a hospital with sepsis, a correlation was found between TNFα and IL-6 levels and septic complications (Terregino et al., 2000, Ann. Emerg. Med., 35, 26). TNFα has also been implicated in cachexia and muscle degradation, associated with HIV infection (Lahdiverta et al., 1988, Amer. J. Med., 85, 289). Obesity is associated with an increase incidence of infection, diabetes and cardiovascular disease. Abnormalities in TNFα expression have been noted for each of the above conditions (Loffreda, et al., 1998, FASEB J. 12, 57). It has been proposed that elevated levels of TNFα are involved in other eating related disorders such as anorexia and bulimia nervosa. Pathophysiological parallels are drawn between anorexia nervosa and cancer cachexia (Holden, et al., 1996, Med Hypotheses 47, 423). An inhibitor of TNFα production, HU-211, was shown to improve the outcome of closed brain injury in an experimental model (Shohami, et al., 1997, J Neuroimmunol. 72, 169). Atherosclerosis is known to have an inflammatory component and cytokines such as IL-1 and TNF have been suggested to promote the disease. In an animal model an IL-1 receptor antagonist was shown to inhibit fatty streak formation (Elhage et al., 1998, Circulation, 97, 242).

TNFα levels are elevated in airways of patients with chronic obstructive pulmonary disease and it may contribute to the pathogenesis of this disease (M. A. Higham et al, 2000, Eur. Respiratory J., 15, 281). Circulating TNFα may also contribute to weight loss associated with this disease (N. Takabatake et al., 2000, Amer. J. Resp. & Crit. Care Med., 161 (4 Pt 1), 1179). Elevated TNFα levels have also been found to be associated with congestive heart failure and the level has been correlated with severity of the disease (A. M. Feldman et al, 2000, J. Amer. College of Cardiology, 35, 537). In addition, TNFα has been implicated in reperfusion injury in lung (Borjesson et al., 2000, Amer. J. Physiol., 278, L3-12), kidney (Lemay et al., 2000, Transplantation, 69, 959), and the nervous system (Mitsui et al., 1999, Brain Res., 844, 192).

TNFα is also a potent osteoclastogenic agent and is involved in bone resorption and diseases involving bone resorption (Abu-Amer et al., 2000, J. Biol. Chem., 275, 27307). It has also been found highly expressed in chondrocytes of patients with traumatic arthritis (Melchiorri et al., 2000, Arthritis and Rheumatism, 41, 2165). TNFα has also been shown to play a key role in the development of glomerulonephritis (Le Hir et al., 1998, Laboratory Investigation, 78, 1625).

The abnormal expression of inducible nitric oxide synthetase (iNOS) has been associated with hypertension in the spontaneously hypertensive rat (Chou et al., 1998, Hypertension, 31, 643). IL-1 has a role in the expression of iNOS and therefore may also have a role in the pathogenesis of hypertension (Singh et al., 1996, Amer. J. Hypertension, 9, 867).

IL-1 has also been shown to induce uveitis in rats which could be inhibited with IL-1 blockers. (Xuan et al., 1998, J. Ocular Pharmacol. and Ther., 14, 31). Cytokines including IL-1, TNF and GM-CSF have been shown to stimulate proliferation of acute myelogenous leukemia blasts (Bruserud, 1996, Leukemia Res. 20, 65). IL-1 was shown to be essential for the development of both irritant and allergic contact dermatitis. Epicutaneous sensitization can be prevented by the administration of an anti-IL-1 monoclonal antibody before epicutaneous application of an allergen (Muller, et al., 1996, Am J Contact Dermat. 7, 177). Data obtained from IL-1 knock out mice indicates the critical involvement in fever for this cytokine (Kluger et al., 1998, Clin Exp Pharmacol Physiol. 25, 141). A variety of cytokines including TNF, IL-1, IL-6 and IL-8 initiate the acute-phase reaction which is stereotyped in fever, malaise, myalgia, headaches, cellular hypermetabolism and multiple endocrine and enzyme responses (Beisel, 1995, Am J Clin Nutr. 62, 813). The production of these inflammatory cytokines rapidly follows trauma or pathogenic organism invasion.

Other proinflammatory cytokines have been correlated with a variety of disease states. IL-8 correlates with influx of neutrophils into sites of inflammation or injury. Blocking antibodies against IL-8 have demonstrated a role for IL-8 in the neutrophil associated tissue injury in acute inflammation (Harada et al, 1996, Molecular Medicine Today 2, 482). Therefore, an inhibitor of IL-8 production may be useful in the treatment of diseases mediated predominantly by neutrophils such as stroke and myocardial infarction, alone or following thrombolytic therapy, thermal injury, adult respiratory distress syndrome (ARDS), multiple organ injury secondary to trauma, acute glomerulonephritis, dermatoses with acute inflammatory components, acute purulent meningitis or other central nervous system disorders, hemodialysis, leukopherisis, granulocyte transfusion associated syndromes, and necrotizing enterocolitis. Rhinovirus triggers the production of various proinflammatory cytokines, predominantly IL-8, which results in symptomatic illnesses such as acute rhinitis (Winther et al., 1998, Am J Rhinol. 12, 17).

Other diseases that are effected by IL-8 include myocardial ischemia and reperfusion, inflammatory bowel disease and many others.

The proinflammatory cytokine IL-6 has been implicated with the acute phase response. IL-6 is a growth factor in a number in oncological diseases including multiple myeloma and related plasma cell dyscrasias (Treon, et al., 1998, Current Opinion in Hematology 5: 42). It has also been shown to be an important mediator of inflammation within the central nervous system. Elevated levels of IL-6 are found in several neurological disorders including AIDS dementia complex, Alzheimer's disease, multiple sclerosis, systemic lupus erythematosus, CNS trauma and viral and bacterial meningitis (Gruol, et al., 1997, Molecular Neurobiology 15: 307). IL-6 also plays a significant role in osteoporosis. In murine models it has been shown to effect bone resorption and to induce osteoclast activity (Ershler et al., 1997, Development and Comparative Immunol. 21: 487). Marked cytokine differences, such as IL-6 levels, exist in vivo between osteoclasts of normal bone and bone from patients with Paget's disease (Mills, et al., 1997, Calcif Tissue Int. 61, 16). A number of cytokines have been shown to be involved in cancer cachexia. The severity of key parameters of cachexia can be reduced by treatment with anti IL-6 antibodies or with IL-6 receptor antagonists (Strassmann, et al., 1995, Cytokins Mol Ther. 1, 107). Several infectious diseases, such as influenza, indicate IL-6 and IFN alpha as key factors in both symptom formation and in host defense (Hayden, et al., 1998, J Clin Invest. 101, 643). Overexpression of IL-6 has been implicated in the pathology of a number of diseases including multiple myeloma, rheumatoid arthritis, Castleman's disease, psoriasis and post-menopausal osteoporosis (Simpson, et al., 1997, Protein Sci. 6, 929). Compounds that interfered with the production of cytokines including IL-6, and TNF were effective in blocking a passive cutaneous anaphylaxis in mice (Scholz et al., 1998, J. Med. Chem., 41, 1050).

GM-CSF is another proinflammatory cytokine with relevance to a number of therapeutic diseases. It influences not only proliferation and differentiation of stem cells but also regulates several other cells involved in acute and chronic inflammation. Treatment with GM-CSF has been attempted in a number of disease states including bum-wound healing, skin-graft resolution as well as cytostatic and radiotherapy induced mucositis (Masucci, 1996, Medical Oncology 13: 149). GM-CSF also appears to play a role in the replication of human immunodeficiency virus (HIV) in cells of macrophage lineage with relevance to AIDS therapy (Crowe et al., 1997, Journal of Leukocyte Biology 62, 41). Bronchial asthma is characterised by an inflammatory process in lungs. Involved cytokines include GM-CSF amongst others (Lee, 1998, J R Coll Physicians Lond 32, 56).

Interferon γ (IFNγ) has been implicated in a number of diseases. It has been associated with increased collagen deposition that is a central histopathological feature of graft-versus-host disease (Parkman, 1998, Curr Opin Hematol. 5, 22). Following kidney transplantation, a patient was diagnosed with acute myelogenous leukemia. Retrospective analysis of peripheral blood cytokines revealed elevated levels of GM-CSF and IFNγ. These elevated levels coincided with a rise in peripheral blood white cell count (Burke, et al., 1995, Leuk Lymphoma. 19, 173). The development of insulin-dependent diabetes (Type 1) can be correlated with the accumulation in pancreatic islet cells of T-cells producing IFNγ (Ablumunits, et al., 1998, J Autoimmun. 11, 73). IFNγ along with TNF, IL-2 and IL-6 lead to the activation of most peripheral T-cells prior to the development of lesions in the central nervous system for diseases such as multiple sclerosis (MS) and AIDS dementia complex (Martino et al., 1998, Ann Neurol. 43, 340). Atherosclerotic lesions result in arterial disease that can lead to cardiac and cerebral infarction. Many activated immune cells are present in these lesions, mainly T-cells and macrophages. These cells produce large amounts of proinflammatory cytokines such as TNF, IL-1 and IFNγ. These cytokines are thought to be involved in promoting apoptosis or programmed cell death of the surrounding vascular smooth muscle cells resulting in the atherosclerotic lesions (Geng, 1997, Heart Vessels Suppl 12, 76). Allergic subjects produce mRNA specific for IFNγ following challenge with Vespula venom (Bonay, et al., 1997, Clin Exp Immunol. 109, 342). The expression of a number of cytokines, including IFNγ has been shown to increase following a delayed type hypersensitivity reaction thus indicating a role for IFNγ in atopic dermatitis (Szepietowski, et al., 1997, Br J Dermatol. 137, 195). Histopathologic and immunohistologic studies were performed in cases of fatal cerebral malaria. Evidence for elevated IFNγ amongst other cytokines was observed indicating a role in this disease (Udomsangpetch et al., 1997, Am J Trop Med Hyg. 57, 501). The importance of free radical species in the pathogenesis of various infectious diseases has been established. The nitric oxide synthesis pathway is activated in response to infection with certain viruses via the induction of proinflammatory cytokines such as IFNγ (Akaike, et al., 1998, Proc Soc Exp Biol Med. 217, 64). Patients, chronically infected with hepatitis B virus (HBV) can develop cirrhosis and hepatocellular carcinoma. Viral gene expression and replication in HBV transgenic mice can be suppressed by a post-transcriptional mechanism mediated by IFN γ, TNF and IL-2 (Chisari, et al., 1995, Springer Semin Immunopathol 17, 261). IFNγ can selectively inhibit cytokine induced bone resorption. It appears to do this via the intermediacy of nitric oxide (NO) which is an important regulatory molecule in bone remodeling. NO may be involved as a mediator of bone disease for such diseases as: the rheumatoid arthritis, tumor associated osteolysis and postmenopausal osteoporosis (Evans, et al, 1996, J Bone Miner Res. 11, 300). Studies with gene deficient mice have demonstrated that the IL-12 dependent production of IFNγ is critical in the control of early parasitic growth. Although this process is independent of nitric oxide the control of chronic infection does appear to be NO dependent (Alexander et al., 1997, Philos Trans R Soc Lond B Biol Sci 352, 1355). NO is an important vasodilator and convincing evidence exists for its role in cardiovascular shock (Kilboum, et al., 1997, Dis Mon. 43, 277). IFNγ is required for progression of chronic intestinal inflammation in such diseases as Crohn's disease and inflammatory bowel disease (IBD) presumably through the intermediacy of CD4+lymphocytes probably of the TH1 phenotype (Sartor 1996, Aliment Pharmacol Ther. 10 Suppl 2, 43). An elevated level of serum IgE is associated with various atopic diseases such as bronchial asthma and atopic dermatitis. The level of IFNγ was negatively correlated with serum IgE suggesting a role for IFNγ in atopic patients (Teramoto et al., 1998, Clin Exp Allergy 28, 74).

WO 01/01986 discloses particular compounds alleged to having the ability to inhibit TNF-alpha. The specific inhibitors disclosed are structurally distinct from the novel compounds disclosed in the present application disclosed hereinbelow. Certain compounds disclosed in WO 01/01986 are indicated to be effective in treating the following diseases: dementia associated with HIV infection, glaucoma, optic-neuropathy, optic neuritis, retinal ischemia, laser induced optic damage, surgery or trauma-induced proliferative vitreoretinopathy, cerebral ischemia, hypoxia-ischemia, hypoglycemia, domoic acid poisoning, anoxia, carbon monoxide or manganese or cyanide poisoning, Huntington's disease, Alzheimer's disease, Parkinson's disease, meningitis, multiple sclerosis and other demyelinating diseases, amyotrophic lateral sclerosis, head and spinal cord trauma, seizures, convulsions, olivopontocerebellar atrophy, neuropathic pain syndromes, diabetic neuropathy, HIV-related neuropathy, MERRF and MELAS syndromes, Leber's disease, Wemicke's encephalophathy, Rett syndrome, homocysteinuria, hyperprolinemia, hyperhomocysteinemia, nonketotic hyperglycinemia, hydroxybutyric aminoaciduria, sulfite oxidase deficiency, combined systems disease, lead encephalopathy, Tourett's syndrome, hepatic encephalopathy, drug addiction, drug tolerance, drug dependency, depression, anxiety and schizophrenia. WO 02/32862 discloses that inhibitors of pro-inflammatory cytokines including TNFα are allegedly useful for treating acute and chronic inflammation in the lung caused by inhalation of smoke such as cigarette smoke. TNFα anatagonists are apparently also useful for the treatment of endometriosis, see EP 1022027 A1. Infliximab, in clinical trials for RA, has also been indicated to be useful for treating various inflammatory diseases including Behcet's disease, uveitis and ankylosing spondylitis. Pancreatitis may also be regulated by inflammatory mediator production, see J Surg Res 2000 May 15 90(2)95-101; Shock 1998 September. 10(3):160-75. p38MAPkinase pathway plays an role in B.burgdorferi-elicited infammation and may be useful in treating inflammation induced by the Lyme disease agent. Anguita, J. et. al., The Journal of Immunology, 2002, 168:6352-6357.

Anti-cytokine drugs may also have therapeutic utility in treating tumor cells. Drug Resistance Updates 4(4):253-267, 2001 August. WO 02/38143 discloses the use of p38 inhibitors to enhance the efficacy and safety of genotoxic therapy for treating, for example, aging, cancer and certain types of heart failure.

Compounds which modulate release of one or more of the aforementioned inflammatory cytokines can be useful in treating diseases associated with release of these cytokines. For example, WO 98/52558 discloses heteroaryl urea compounds which are indicated to be useful in treating cytokine mediated diseases. WO 99/23091 discloses another class of urea compounds which are useful as anti-inflammatory agents. WO 99/32463 relates to aryl ureas amd their use in treating cytokine diseases and proteolytic enzyme mediated disease. WO 00/41698 discloses aryl ureas said to be useful in treating p38 MAP kinase diseases.

U.S. Pat. No. 5,162,360 discloses N-substituted aryl-N′-heterocyclic substituted urea compounds which are described as being useful for treating hypercholesterolemia and atheroclerosis.

The work cited above supports the principle that inhibition of cytokine production will be beneficial in the treatment acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure. None of these specific diseases have been taught or described in WO 00/55139 as being possible indications for the compounds taught therein. Therefore a need exists for small molecule inhibitors for treating these diseases with optimized efficacy, pharmacokinetic and safety profiles.

BRIEF SUMMARY OF THE INVENTION

The present invention is directed a method of treating a cytokine mediated disease or condition chosen from: acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme Disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of compounds disclosed in in WO 00/55139.

DETAILED DESCRIPTION OF THE INVENTION

In a first broad generic aspect, the present invention is directed a method of treating a cytokine mediated disease or condition chosen from: acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the formula (I) disclosed in WO 00/55139 which is the PCT case of U.S. application Ser. No. 09/505,582 (both of which are incorporated by reference herein in it their entirety):

-   -   wherein:     -   Ar₁ is selected from the group consisting of:         pyrrole, pyrrolidine, pyrazole, imidazole, oxazole, thiazole,         furan and thiophene; wherein Ar₁ may be substituted by one or         more R₁, R₂ or R₃;     -   Ar₂ is:         phenyl, naphthyl, quinoline, isoquinoline, tetrahydronaphthyl,         tetrahydroquinoline, tetrahydroisoquinoline, benzimidazole,         benzofuran, indanyl, indenyl or indole each being optionally         substituted with zero to three R₂ groups;     -   X is:

-   a) a C₅₋₈ cycloalkyl or cycloalkenyl optionally substituted with 0-2     oxo groups or 0-3 C₁₋₄ branched or unbranched alkyl, C₁₋₄ alkoxy or     C₁₋₄ alkylamino chains;

-   b) phenyl, furan, thiophene, pyrrole, imidazolyl, pyridine,     pyrimidine, pyridinone, dihydropyridinone, maleimide,     dihydromaleimide, piperdine, piperazine or pyrazine each being     optionally independently substituted with 0-3 C₁₋₄ branched or     unbranched alkyl, C₁₋₄alkoxy, hydroxy, nitrile, mono- or di-(C₁₋₃     alkyl)amino, C₁₋₆ alkyl-S(O)_(m), or halogen;     -   Y is:         a bond or a C₁₋₄ saturated or unsaturated branched or unbranched         carbon chain optionally partially or fully halogenated, wherein         one or more methylene groups are optionally replaced by O, NH,         S(O), S(O)₂ or S and wherein Y is optionally independently         substituted with 0-2 oxo groups and one or more C₁₋₄ branched or         unbranched alkyl which may be substituted by one or more halogen         atoms;     -   Z is:

-   a) phenyl, pyridine, pyrimidine, pyridazine, imidazole, furan,     thiophene, pyran, which are optionally substituted with one to three     groups consisting of halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, hydroxy,     mono- or di-(C₁₋₃ alkyl)amino, C₁₋₆ alkyl-S(O)_(m), COOH and     phenylamino wherein the phenyl ring is optionally substituted with     one to two groups consisting of halogen, C₁₋₆ alkyl and C₁₋₆ alkoxy;

-   b) tetrahydropyran, tetrahydrofuran, 1,3-dioxolanone, 1,3-dioxanone,     1,4-dioxane, morpholine, thiomorpholine, thiomorpholine sulfoxide,     piperidine, piperidinone, piperazine, tetrahydropyrimidone,     cyclohexanone, cyclohexanol, pentamethylene sulfide, pentamethylene     sulfoxide, pentamethylene sulfone, tetramethylene sulfide,     tetramethylene sulfoxide or tetramethylene sulfone which are     optionally substituted with one to three groups consisting of     nitrile, C₁₋₆ alkyl, C₁₋₆ alkoxy, hydroxy, mono- or di-(C₁₋₃     alkyl)amino-C₁₋₃ alkyl, phenylamino-C₁₋₃ alkyl and C₁₋₃ alkoxy-C₁₋₃     alkyl;

-   c) C₁₋₆ alkoxy, secondary or tertiary amine wherein the amino     nitrogen is covalently bonded to groups selected from the group     consisting of C₁₋₃ alkyl, C₁₋₅ alkoxyalkyl, pyridinyl-C₁₋₃ alkyl,     imidazolyl-C₁₋₃ alkyl, tetrahydrofuranyl-C₁₋₃ alkyl, phenylamino,     wherein the phenyl ring is optionally substituted with one to two     halogen, C₁₋₆ alkoxy, hydroxy or mono- or di-(C₁₋₃ alkyl)amino, C₁₋₆     alkyl-S(O)_(m), and phenyl-S(O)_(m), wherein the phenyl ring is     optionally substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy     or mono- or di-(C₁₋₃ alkyl)amino;     -   R₁ is:

-   (a) C₃₋₁₀ branched or unbranched alkyl optionally partially or fully     halogenated and optionally substituted with one to three phenyl,     naphthyl or heterocyclic groups selected from the group consisting     of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl,     imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl and isothiazolyl;     each such phenyl, naphthyl or heterocycle selected from the group     hereinabove described in this paragraph, and being substituted with     0 to 5 groups selected from the group consisting of halogen, C₁₋₆     branched or unbranched alkyl which is optionally partially or fully     halogenated, C₃₋₈ cycloalkyl, C₅₋₈ cycloalkenyl, hydroxy, nitrile,     C₁₋₃ alkyloxy which is optionally partially or fully halogenated,     NH₂C(O) and di(C₁₋₃)alkylaminocarbonyl;

-   (b) C₃₋₇ cycloalkyl selected from the group consisting of     cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, cycloheptanyl,     bicyclopentanyl, bicyclohexanyl and bicycloheptanyl each being     optionally be partially or fully halogenated and optionally     substituted with one to three C₁₋₃ alkyl groups, or an analog of     such cycloalkyl group wherein one to three ring methylene groups are     replaced by groups independently selected from the group consisting     of O, S, CHOH, >C═O, >C═S and NH;

-   (c) C₃₋₁₀ branched alkenyl optionally partially or fully halogenated     and optionally substituted with one to three C₁₋₅ branched or     unbranched alkyl, phenyl, naphthyl or heterocyclic groups, with each     such heterocyclic group being independently selected from the group     consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl,     pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl and     isothiazolyl, and each such phenyl, naphthyl or heterocyclic group     being substituted with 0 to 5 groups selected from the group     consisting of halogen, C₁₋₆ branched or unbranched alkyl which is     optionally partially or fully halogenated, cyclopropyl, cyclobutyl,     cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl,     bicyclohexanyl, bicycloheptanyl, hydroxy, nitrile, C₁₋₃ alkoxy which     is optionally partially or fully halogenated, NH₂C(O) and mono- or     di(C₁₋₃)alkylaminocarbonyl;

-   (d) a C₅₋₇ cycloalkenyl selected from the group consisting of     cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,     cycloheptadienyl, bicyclohexenyl and bicycloheptenyl, wherein such     cycloalkenyl group is optionally substituted with one to three C₁₋₃     alkyl groups;

-   (e) nitrile; or

-   (f) C₁₋₆ branched or unbranched alkoxycarbonyl, C₁₋₆ branched or     unbranched alkylaminocarbonyl, C₁₋₆ branched or unbranched     alkylcarbonylamino-C₁₋₃-alkyl;     -   R₂ is:         a C₁₋₆ branched or unbranched alkyl optionally partially or         fully halogenated, acetyl, aroyl, C₁₋₄ branched or unbranched         alkoxy optionally partially or fully halogenated, halogen,         methoxycarbonyl or phenylsulfonyl;     -   R₃ is:

-   a) phenyl, naphthyl or heterocyclic group selected from the group     consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl,     pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, tetrahydrofuryl,     isoxazolyl, isothiazolyl, quinolinyl, isoquinolinyl, indolyl,     benzimidazolyl, benzofuranyl, benzoxazolyl, benzisoxazolyl,     benzpyrazolyl, benzothiofuranyl, cinnolinyl, pterindinyl,     phthalazinyl, naphthypyridinyl, quinoxalinyl, quinazolinyl, purinyl     and indazolyl, wherein such phenyl, naphthyl or heterocyclic group     is optionally substituted with one to five groups selected from the     group consisting of phenyl, naphthyl, heterocycle selected from the     group hereinabove described in this paragraph, C₁₋₆ branched or     unbranched alkyl which is optionally partially or fully halogenated,     cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl,     bicyclopentyl, bicyclohexyl, bicycloheptyl, phenyl C₁₋₅ alkyl,     naphthyl C₁₋₅ alkyl, halogen, hydroxy, nitrile, C₁₋₃ alkyloxy which     may optionally be partially or fully halogenated, phenyloxy,     naphthyloxy, heteraryloxy wherein the heterocyclic moiety is     selected from the group hereinabove described in this paragraph,     nitro, amino, mono- or di-(C₁₋₃)alkylamino, phenylamino,     naphthylamino, heterocyclylamino wherein the heterocyclyl moiety is     selected from the group hereinabove described in this paragraph,     NH₂C(O), a mono- or di-(C₁₋₃)alkyl aminocarbonyl, C₁₋₅     alkyl-C(O)—C₁₋₄ alkyl, amino-C₁₋₅ alkyl, mono- or     di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, amino-S(O)₂,     di-(C₁₋₃)alkylamino-S(O)₂, R₄—C₁₋₅ alkyl, R₅—C₁₋₅ alkoxy,     R₆—C(O)—C₁₋₅ alkyl and R₇—C₁₋₅ alkyl(R₈)N, carboxy-mono- or     di-(C₁₋₅)-alkyl-amino;

-   b) a fused aryl selected from the group consisting of     benzocyclobutanyl, indanyl, indenyl, dihydronaphthyl,     tetrahydronaphthyl, benzocycloheptanyl and benzocycloheptenyl, or a     fused heterocyclyl selected from the group consisting of     cyclopentenopyridine, cyclohexanopyridine, cyclopentanopyrimidine,     cyclohexanopyrimidine, cyclopentanopyrazine, cyclohexanopyrazine,     cyclopentanopyridazine, cyclohexanopyridazine,     cyclopentanoquinoline, cyclohexanoquinoline,     cyclopentanoisoquinoline, cyclohexanoisoquinoline,     cyclopentanoindole, cyclohexanoindole, cyclopentanobenzimidazole,     cyclohexanobenzimidazole, cyclopentanobenzoxazole,     cyclohexanobenzoxazole, cyclopentanoimidazole, cyclohexanoimidazole,     cyclopentanothiophene and cyclohexanothiophene; wherein the fused     aryl or fused heterocyclyl ring is substituted with 0 to 3 groups     independently selected from the group consisting of phenyl, naphthyl     and heterocyclyl selected from the group consisting of pyridinyl,     pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl,     pyrazolyl, thienyl, furyl, isoxazolyl, and isothiazolyl, C₁₋₆     branched or unbranched alkyl which is optionally partially or fully     halogenated, halogen, nitrile, C₁₋₃ alkoxy which is optionally     partially or fully halogenated, phenyloxy, naphthyloxy,     heterocyclyloxy wherein the heterocyclyl moiety is selected from the     group hereinabove described in this paragraph, nitro, amino, mono-     or di-(C₁₋₃)alkylamino, phenylamino, naphthylamino,     heterocyclylamino wherein the heterocyclyl moiety is selected from     the group hereinabove described in this paragraph, NH₂C(O), a mono-     or di-(C₁₋₃)alkyl aminocarbonyl, C₁₋₄ alkyl-OC(O), C₁₋₅     alkyl-C(O)-C₁₋₄ branched or unbranched alkyl, an amino-C₁₋₅ alkyl,     mono- or di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, R₉—C₁₋₅ alkyl, R₁₀—C₁₋₅     alkoxy, R₁₁—C(O)—C₁₋₅ alkyl, and R₁₂—C₁₋₅ alkyl(R₁₃)N;

-   c) cycloalkyl selected from the group consisting of cyclopentyl,     cyclohexyl, cycloheptyl, bicyclopentyl, bicyclohexyl and     bicycloheptyl, wherein the cycloalkyl is optionally partially or     fully halogenated and optionally substituted with one to three C₁₋₃     alkyl groups;

-   d) C₅₋₇ cycloalkenyl selected from the group consisting of     cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,     cycloheptadienyl, bicyclohexenyl and bicycloheptenyl, wherein such     cycloalkenyl group is optionally substituted with one to three C₁₋₃     alkyl groups;

-   e) acetyl, aroyl, alkoxycarbonylalkyl or phenylsulfonyl; or

-   f) C₁₋₆ branched or unbranched alkyl optionally partially or fully     halogenated;     or R₁ and R₂ taken together may optionally form a fused phenyl or     pyridinyl ring;     -   each R₈ and R₁₃ is independently selected from the group         consisting of: hydrogen and C₁₋₄ branched or unbranched alkyl         optionally be partially or fully halogenated;     -   each R₄, R₅, R₆, R₇, R₉, R₁₀, R₁₁ and R₁₂ is independently         selected from the group consisting of morpholine, piperidine,         piperazine, imidazole and tetrazole;

-   m is 0, 1 or 2;

-   W is O or S and     the pharmaceutically acceptable derivatives thereof.

A preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I) as provided above and wherein:

-   -   Ar₂ is naphthyl, tetrahydronaphthyl, indanyl or indenyl and     -   W is O.

A more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I) as provided above and wherein:

-   -   Ar₁ is selected from thiophene and pyrazole;     -   X is C₅₋₇ cycloalkyl or C₅₋₇cycloalkenyl optionally substituted         with 0-2 oxo groups or 0-3 C₁₋₄ branched or unbranched alkyl,         C₁₋₄ alkoxy or C₁₋₄ alkylamino; or X is phenyl, pyridine,         tetrahydropyridine, pyrimidine, furan or thiophene each being         optionally independently substituted with 0-3 C₁₋₄ branched or         unbranched alkyl, C₁₋₄alkoxy, hydroxy, nitrile, mono- or         di-(C₁₋₃ alkyl)amino, C₁₋₆ alkyl-S(O)_(m) or halogen;     -   R₁ is C₁₋₄alkyl branched or unbranched, cyclopropyl or         cyclohexyl optionally partially or fully halogenated and         optionally substituted with one to three C₁₋₃ alkyl groups;     -   R₃ is C₁₋₄alkyl branched or unbranched, phenyl, pyrimidinyl,         pyrazolyl or pyridinyl each being optionally substituted as         described hereinabove in the broadest generic aspect,         alkoxycarbonylalkyl or cyclopropyl or cyclopentyl optionally         substituted as described hereinabove in the broadest generic         aspect.

A yet more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I), as described in the immediate previous paragraph, wherein:

-   -   Ar₁ is pyrazole;     -   X is cyclopentenyl, cyclohexenyl or cycloheptenyl, optionally         substituted with an oxo group or 0-3 C₁₋₄ branched or unbranched         alkyl, C₁₋₄alkoxy or C₁₋₄alkylamino; or X is phenyl, pyridine,         furan or thiophene each being optionally independently         substituted with 0-3 C₁₋₄ branched or unbranched alkyl,         C₁₋₄alkoxy, hydroxy, nitrile, mono- or di-(C₁₋₃ alkyl)amino,         C₁₋₆ alkyl-S(O)_(m) or halogen.

A yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I), as described in the immediate previous paragraph, and wherein:

-   -   Y is —CH2—, —CH2CH2—, —CH2NH—, —CH2CH2NH— or a bond; and     -   Z is         phenyl, imidazole, furan, piperazine, tetrahydropyran,         morpholine, thiomorpholine, thiomorpholine sulfoxide,         piperidine, pyridine, secondary or tertiary amine wherein the         amino nitrogen is covalently bonded to groups selected from the         group consisting of C₁₋₃ alkyl and C₁₋₅ alkoxyalkyl, phenylamino         wherein the phenyl ring is optionally substituted with one to         two halogen, C₁₋₆ alkoxy, hydroxy or mono- or di-(C₁₋₃         alkyl)amino, C₁₋₆ alkyl-S(O)_(m) and phenyl-S(O)_(m) wherein the         phenyl ring is optionally substituted with one to two halogen,         C₁₋₆ alkoxy, hydroxy or mono- or di-(C₁₋₃ alkyl)amino.

A further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I), as described in the immediate previous paragraph, and wherein:

-   -   Ar₁ is 5-tert-butyl-pyrazol-3-yl; wherein the pyrazole ring may         be substituted by R₃;     -   R₃ is C₁₋₄alkyl branched or unbranched, phenyl, pyrimidinyl,         pyrazolyl, pyridinyl each being optionally substituted as         described hereinabove in the broadest generic aspect,         alkoxycarbonylalkyl or cyclopropyl or cyclopentyl optionally         substituted as described hereinabove in the broadest generic         aspect.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I), as described in the immediate previous paragraph, and wherein:

X is pyridinyl.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (I), as described in the immediate previous paragraph, and wherein:

the pyridinyl is attached to Ar₁ via the 3-pyridinyl position.

The following compounds are representative of the compounds of formula (I) which may be useful in the novel methods described herein:

-   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(2-(morpholin-4-yl)ethyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-dimethylaminophenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-morpholin-4-ylmethyl-pyridin-2-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-morpholin-4-ylmethyl-fur-2-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-methyl-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-phenyl-2H-pyrazol-3-yl]-3-[4-(4-piperdin-1-ylmethyl-phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-phenyl-2H-pyrazol-3-yl]-3-[4-(4-(4-methylpiperazin-1-yl)methylphenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3,4-di(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-pyridin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-     thiomorpholin-4-ylmethyl)pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-thiomorpholin-4-ylmethyl)pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-tetrahydropyran-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-tetrahydrothiophen-3-ylmethyl)pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(imidazol-1-ylmethyl)pyridin-3-yl)naphthalen-1-yl]urea; -   1-[2-(3-dimethylaminomethylphenyl)-5-(1-methyl-cyclohexyl)-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[2-(5-(1-methyl-cyclohexyl)-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-methoxy-5-(2-morpholin-4-yl-ethoxy)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-morpholin-4-yl-ethoxy)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-3-(dimethylamino)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-3-(methylsulfonyl)phenyl)naphthalen-1-yl]urea; -   5-tert-butyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]ureido}thiophene-2-carboxylic     acid methyl ester; -   5-tert-butyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]ureido}thiophene-2-carboxylic     acid methylamide; -   5-tert-butyl-1-methyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]ureido}-1H-pyrrole-2-carboxylic     acid methyl ester; -   5-tert-butyl-1-methyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]ureido}-1H-pyrrole-2-carboxylic     acid methylamide; -   2-acetylamino     N-(5-tert-butyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]ureido}thiophen-2-ylmethyl)acetamide; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-morpholin-4-yl-cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-morpholin-4-yl-cylohept-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-(2-morpholin-4-yl-ethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-morpholin-4-yl-cyclohept-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(pyridin-4-yl-methylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(dimethylaminoethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(pyridin-3-yl-methylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(phenyl-methylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-phenylethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(furan-2-yl-methylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-pyridin-2-yl-ethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-piperdin-1-yl-ethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-imidazol-4-yl-ethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(pyridin-2-yl-     methylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-(4-methoxyphenyl)ethylamino)cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-morpholin-4-ylmethyl-3-oxo-cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(1-oxo-tetrahydrothiophen-3-ylmethyl)-3-oxo-cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(1-oxo-thiomorpholin-4-ylmethyl)-3-oxo-cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-methylpiperazin-1-ylmethyl)-3-oxo-cyclohex-1-enyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-{6-oxo-1-(tetrahydro-pyran-4-ylmethyl)-1,2,3,6-tetrahydro-pyridin-4-yl}naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(2-oxo-1-pyridin-4-ylmethyl-piperdin-4-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-oxo-1-pyridin-4-yl-1,2,3,6-tetrahydro-pyridin-4-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-oxo-1-pyridin-4-yl-1,2,3,6-tetrahydro-pyridin-4-yl)naphthalen-1-yl]urea; -   5-tert-butyl-3-{3-[4-(6-oxo-1-pyridin-4-yl-1,2,3,6-tetrahydro-pyridin-4-yl)naphthalen-1-yl]ureido}thiophene-2-carboxylic     acid methyl ester; -   5-tert-butyl-1-methyl-3-{3-[4-(6-oxo-1-pyridin-4-yl-1,2,3,6-tetrahydro-pyridin-4-yl)naphthalen-1-yl]ureido}pyrrole-2-carboxylic     acid methyl ester; -   5-tert-butyl-1-methyl-3-{3-[4-(6-oxo-1-pyridin-4-yl-1,2,3,6-tetrahydro-pyridin-4-yl)naphthalen-1-yl]ureido}pyrrole-2-carboxylic     acid methyl amide; -   5-tert-butyl-3-{3-[4-(3-morpholin-4-yl-cyclohex-1-enyl)naphthalen-1-yl]ureido}thiophene-2-carboxylic     acid methyl ester; -   5-tert-butyl-1-methyl-3-{3-[4-(3-morpholin-4-yl-cyclohex-1-enyl)naphthalen-1-yl]ureido}pyrrole-2-carboxylic     acid methyl ester; and -   5-tert-butyl-1-methyl-3-{3-[4-(3-morpholin-4-yl-cyclohex-1-enyl)naphthalen-1-yl]ureido}pyrrole-2-carboxylic     acid methyl amide and     the pharmaceutically acceptable derivatives thereof.

In another embodiment of the invention there are provided the following compounds of formula (I) which may be useful in the novel methods described herein:

-   1-[5-tert-butyl-2-(2-methoxypyridin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylthiopyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methoxypyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-methyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-(3-methylsulfanylpropyl)-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-methyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methoxypyridin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(pyridin-3-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(2-(morpholin-4-yl)ethyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-morpholin-4-ylmethyl-pyridin-2-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-morpholin-4-ylmethyl-fur-2-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea; -   1-[5-tert-butyl-2-methyl-2H-pyrazol-3-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)naphthalen-1-yl]urea     and     the pharmaceutically acceptable derivatives thereof.

In a second broad generic aspect, there is provided a method of treating a cytokine mediated disease or condition chosen from: acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the formula (Ia) disclosed in WO 00/55139 which is the PCT case of U.S. application Ser. No. 09/505,582:

-   -   wherein:     -   Ar₁ is:         pyrrole, pyrrolidine, pyrazole, imidazole, oxazole, thiazole,         furan and thiophene; wherein Ar₁ is optionally substituted by         one or more R₁, R₂ or R₃;     -   Ar₂ is:         phenyl, naphthyl, quinoline, isoquinoline, tetrahydronaphthyl,         tetrahydroquinoline, tetrahydroisoquinoline, benzimidazole,         benzo furan, indanyl, indenyl and indole each being optionally         substituted with zero to three R₂ groups;     -   X is:         a C₅₋₈ cycloalkyl or cycloalkenyl optionally substituted with         one to two oxo groups or one to three C₁₋₄ alkyl, C₁₋₄ alkoxy or         C₁₋₄ alkylamino chains each being branched or unbranched;         phenyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl,         pyridinyl, tetrahydropyridinyl, pyrimidinyl, pyridinonyl,         dihydropyridinonyl, maleimidyl, dihydromaleimidyl, piperdinyl,         benzimidazole, 3H-imidazo[4,5-b]pyridine, piperazinyl,         pyridazinyl or pyrazinyl; each being optionally independently         substituted with one to three C₁₋₄ alkyl, C₁₋₄alkoxy, hydroxy,         nitrile, amino, mono- or di-(C₁₋₃ alkyl)amino, mono- or di-(C₁₋₃         alkylamino)carbonyl, NH₂C(O), C₁₋₆ alkyl-S(O)_(m) or halogen;     -   Y is:         a bond or a C₁₋₄ saturated or unsaturated branched or unbranched         carbon chain optionally partially or fully halogenated, wherein         one or more C atoms are optionally replaced by O, N, or S(O)_(m)         and wherein Y is optionally independently substituted with one         to two oxo groups, nitrile, phenyl, hydroxy or one or more C₁₋₄         alkyl optionally substituted by one or more halogen atoms;     -   Z is:         aryl, indanyl, heteroaryl selected from benzimidazolyl,         pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, imidazolyl,         pyrazolyl, triazolyl, tetrazolyl, furanyl, thienyl and pyranyl,         heterocycle selected from piperazinyl, tetrahydropyrimidonyl,         cyclohexanonyl, cyclohexanolyl, 2-oxa- or         2-thia-5-aza-bicyclo[2.2.1]heptanyl, pentamethylene sulfidyl,         pentamethylene sulfoxidyl, pentamethylene sulfonyl,         tetramethylene sulfidyl, tetramethylene sulfoxidyl or         tetramethylene sulfonyl, tetrahydropyranyl, tetrahydrofuranyl,         1,3-dioxolanonyl, 1,3-dioxanonyl, 1,4-dioxanyl, morpholino,         thiomorpholino, thiomorpholino sulfoxidyl, thiomorpholino         sulfonyl, piperidinyl, piperidinonyl, pyrrolidinyl and         dioxolanyl,         each of the aforementioned Z are optionally substituted with one         to three halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₁₋₃ alkoxy-C₁₋₃         alkyl, C₁₋₆ alkoxycarbonyl, aroyl, heteroaroyl,         heterocycleC₁₋₃acyl wherein the heteroaryl and heterocycle are         as defined hereinabove in this paragraph, C₁₋₃acyl, oxo,         hydroxy, pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃ alkyl,         tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl, nitrile,         carboxy, phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino, amino-S(O)_(m), C₁₋₆         alkyl-S(O)_(m) or phenyl-S(O)_(m) wherein the phenyl ring is         optionally substituted with one to two halogen, C₁₋₆ alkoxy,         hydroxy, halogen or mono- or di-(C₁₋₃ alkyl)amino;         or Z is optionally substituted with one to three amino,         aminocarbonyl or amino-C₁₋₃ alkyl wherein the N atom is         optionally independently mono- or di-substituted by         aminoC₁₋₆alkyl, C₁₋₃alkyl, arylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl,         C₁₋₅ alkoxy, aroyl, C₁₋₃acyl, C₁₋₃alkyl-S(O)_(m)— or         arylC₀₋₃alkyl-S(O)_(m)— each of the aforementioned alkyl and         aryl attached to the amino group is optionally substituted with         one to two halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, hydroxy or mono- or         di-(C₁₋₃ alkyl)amino;         or Z is optionally substituted with one to three aryl,         heterocycle or heteroaryl as hereinabove described in this         paragraph each in turn is optionally substituted by halogen,         C₁₋₆ alkyl or C₁₋₆ alkoxy;         or Z is hydroxy, hydroxyC₁₋₃alkyl, halogen, nitrile, amino         wherein the N atom is optionally independently mono- or         di-substituted by C₁₋₆alkyl, aminoC₁₋₆alkyl, arylC₀₋₃alkyl, C₁₋₅         alkoxyC₁₋₃ alkyl, C₁₋₅ alkoxy, aroyl, C₁₋₃acyl,         C₁₋₃alkyl-S(O)_(m)—, arylC₀₋₃alkyl-S(O)_(m)—, nitrileC₁₋₄alkyl         or C₁₋₃alkoxyC₁₋₃alkyl, each of the aforementioned alkyl and         aryl attached to the amino group is optionally substituted with         one to two halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, hydroxy or mono- or         di-(C₁₋₃ alkyl)amino, C₁₋₆ alkoxyheteroarylC₀₋₃alkyl,         heteroarylC₀₋₃alkyl or heterocycyleC₀₋₃alkyl wherein the         heteroaryl and heterocycle is hereinabove described in this         paragraph,         or Z is C₁₋₆alkyl branched or unbranched, C₁₋₆alkoxy,         C₁₋₃acylamino, nitrileC₁₋₄alkyl, C₁₋₆ alkyl-S(O)_(m), and         phenyl-S(O)_(m), wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino;     -   R₁ is:

-   a) C₁₋₁₀ branched or unbranched alkyl optionally partially or fully     halogenated, and optionally substituted with one to three phenyl,     naphthyl or heterocyclic groups selected from the group consisting     of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl,     imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl and isothiazolyl;     each such phenyl, naphthyl or heterocycle, selected from the group     hereinabove described, being substituted with 0 to 5 groups selected     from the group consisting of halogen, C₁₋₆ branched or unbranched     alkyl which is optionally partially or fully halogenated, C₃₋₈     cycloalkyl, C₅₋₈ cycloalkenyl, hydroxy, nitrile, C₁₋₃ alkyloxy which     is optionally partially or fully halogenated, NH₂C(O) and     di(C₁₋₃)alkylaminocarbonyl;

-   b) C₃₋₇ cycloalkyl selected from the group consisting of     cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl,     bicyclopentyl, bicyclohexyl and bicycloheptyl, each optionally     partially or fully halogenated and optionally substituted with one     to three C₁₋₃ alkyl groups, or an analog of such cycloalkyl group     wherein one to three ring methylene groups are replaced by groups     independently selected from the group consisting of O, S,     CHOH, >C═O, >C═S and NH;

-   c) C₃₋₁₀ branched alkenyl optionally partially or fully halogenated     and optionally substituted with one to three C₁₋₅ branched or     unbranched alkyl, phenyl, naphthyl or heterocyclic groups, with each     such heterocyclic group being independently selected from the group     consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl,     pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl and     isothiazolyl, and each such phenyl, naphthyl or heterocyclic group     being substituted with 0 to 5 groups selected from the group     consisting of halogen, C₁₋₆ branched or unbranched alkyl which is     optionally partially or fully halogenated, cyclopropyl, cyclobutyl,     cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl,     bicyclohexanyl, bicycloheptanyl, hydroxy, nitrile, C₁₋₃ alkoxy which     is optionally partially or fully halogenated, NH₂C(O) and mono- or     di(C₁₋₃)alkylaminocarbonyl;

-   d) a C₅₋₇ cycloalkenyl selected from the group consisting of     cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,     cycloheptadienyl, bicyclohexenyl and bicycloheptenyl, wherein such     cycloalkenyl group is optionally substituted with one to three C₁₋₃     alkyl groups;

-   e) nitrile; or

-   f) C₁₋₆ branched or unbranched alkoxycarbonyl, C₁₋₆ branched or     unbranched alkylaminocarbonyl, C₁₋₆ branched or unbranched     alkylcarbonylamino-C₁₋₃-alkyl;     -   R₂ is:         a C₁₋₆ branched or unbranched alkyl optionally partially or         fully halogenated and optionally substituted with nitrile,         or R₂ is acetyl, aroyl, C₁₋₄ branched or unbranched alkoxy         optionally partially or fully halogenated, halogen,         methoxycarbonyl or phenylsulfonyl;     -   R₃ is:

-   a) phenyl, naphthyl or heterocyclic group selected from the group     consisting of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl,     pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, tetrahydrofuryl,     isoxazolyl, isothiazolyl, quinolinyl, isoquinolinyl, indolyl,     benzimidazolyl, benzofuranyl, benzoxazolyl, benzisoxazolyl,     benzpyrazolyl, benzothiofuranyl, cinnolinyl, pterindinyl,     phthalazinyl, naphthypyridinyl, quinoxalinyl, quinazolinyl, purinyl     and indazolyl, wherein such phenyl, naphthyl or heterocyclic group     is optionally substituted with one to five groups selected from the     group consisting of a phenyl, naphthyl, heterocycle selected from     the group hereinabove described in this paragraph, C₁₋₆ branched or     unbranched alkyl which is optionally partially or fully halogenated,     cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl,     bicyclopentyl, bicyclohexyl, bicycloheptyl, phenyl C₁₋₅ alkyl,     naphthyl C₁₋₅ alkyl, halogen, hydroxy, oxo, nitrile, C₁₋₃ alkoxy     optionally partially or fully halogenated, C₁₋₃ alkoxyC₁₋₅alkyl,     C₁₋₃thioalkyl, C₁₋₃thioalkylC₁₋₅alkyl, phenyloxy, naphthyloxy,     heteraryloxy wherein the heterocyclic moiety is selected from the     group hereinabove described in this paragraph, nitro, amino, mono-     or di-(C₁₋₃)alkylamino, phenylamino, naphthylamino,     heterocyclylamino wherein the heterocyclyl moiety is selected from     the group hereinabove described in this paragraph, NH₂C(O), a mono-     or di-(C₁₋₃)alkyl aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl,     amino-C₁₋₅ alkyl, mono- or di-(C₁₋₃)alkylamino-C₁₋₅ alkyl,     amino-S(O)₂, di-(C₁₋₃)alkylamino-S(O)₂, R₄—C₁₋₅ alkyl, R₅—C₁₋₅     alkoxy, R₆—C(O)—C₁₋₅ alkyl and R₇—C₁₋₅ alkyl(R₈)N, carboxy-mono- or     di-(C₁₋₅)-alkyl-amino;

-   b) a fused aryl selected from the group consisting of     benzocyclobutanyl, indanyl, indenyl, dihydronaphthyl,     tetrahydronaphthyl, benzocycloheptanyl and benzocycloheptenyl, or a     fused heterocyclyl selected from the group consisting of     cyclopentenopyridine, cyclohexanopyridine, cyclopentanopyrimidine,     cyclohexanopyrimidine, cyclopentanopyrazine, cyclohexanopyrazine,     cyclopentanopyridazine, cyclohexanopyridazine,     cyclopentanoquinoline, cyclohexanoquinoline,     cyclopentanoisoquinoline, cyclohexanoisoquinoline,     cyclopentanoindole, cyclohexanoindole, cyclopentanobenzimidazole,     cyclohexanobenzimidazole, cyclopentanobenzoxazole,     cyclohexanobenzoxazole, cyclopentanoimidazole, cyclohexanoimidazole,     cyclopentanothiophene and cyclohexanothiophene; wherein the fused     aryl or fused heterocyclyl ring is substituted with 0 to 3 groups     independently selected from the group consisting of phenyl, naphthyl     and heterocyclyl selected from the group consisting of pyridinyl,     pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl,     pyrazolyl, thienyl, furyl, isoxazolyl, and isothiazolyl, C₁₋₆     branched or unbranched alkyl which is optionally partially or fully     halogenated, halogen, nitrile, C₁₋₃ alkoxy which is optionally     partially or fully halogenated, phenyloxy, naphthyloxy,     heterocyclyloxy wherein the heterocyclyl moiety is selected from the     group hereinabove described, nitro, amino, mono- or     di-(C₁₋₃)alkylamino, phenylamino, naphthylamino, heterocyclylamino     wherein the heterocyclyl moiety is selected from the group     hereinabove described, NH₂C(O), a mono- or di-(C₁₋₃)alkyl     aminocarbonyl, C₁₋₄ alkyl-OC(O), C₁₋₅ alkyl-C(O)—C₁₋₄ branched or     unbranched alkyl, an amino-C₁₋₅ alkyl, mono- or     di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, R₉—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkoxy,     R₁₁—C(O)—C₁₋₅ alkyl and R₁₂—C₁₋₅ alkyl(R₁₃)N;

-   c) cycloalkyl selected from the group consisting of cyclopropyl,     cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, bicyclopentyl,     bicyclohexyl and bicycloheptyl, wherein the cycloalkyl is optionally     partially or fully halogenated and optionally substituted with one     to three C₁₋₃ alkyl groups;

-   d) C₅₋₇ cycloalkenyl selected from the group consisting of     cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,     cycloheptadienyl, bicyclohexenyl and bicycloheptenyl, wherein such     cycloalkenyl group is optionally substituted with one to three C₁₋₃     alkyl groups;

-   e) acetyl, aroyl, C₁₋₆alkoxycarbonylC₁₋₆alkyl or phenylsulfonyl; or

-   f) C₁₋₆ branched or unbranched alkyl optionally partially or fully     halogenated;     or R₁ and R₂ taken together optionally form a fused phenyl or     pyridinyl ring;     -   each R₈ and R₁₃ is independently selected from the group         consisting of: hydrogen and C₁₋₄ branched or unbranched alkyl         optionally partially or fully halogenated;     -   each R₄, R₅, R₆, R₇, R₉, R₁₀, R₁₁ and R₁₂ is independently         selected from the group consisting of morpholine, piperidine,         piperazine, imidazole and tetrazole;

-   m is 0, 1 or 2;

-   W is O or S;     wherein X is directly attached to one or two —Y-Z, and the     pharmaceutically acceptable derivatives thereof.

A preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (Ia) as provided above and wherein:

-   -   Ar₂ is naphthyl, tetrahydronaphthyl, indanyl or indenyl and     -   W is O.

A more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (Ia) as provided above and wherein:

-   -   Ar₁ is thiophene or pyrazole each substituted independently by         one to three R₁, R₂ or R₃;     -   X is:         a C₅₋₇ cycloalkyl or cycloalkenyl optionally substituted with         one to two oxo groups or one to three C₁₋₄ alkyl, C₁₋₄ alkoxy or         C₁₋₄ alkylamino chains each being branched or unbranched;         phenyl, indanyl, furanyl, thienyl, imidazolyl, pyridinyl,         pyrazinyl, tetrahydrapyridinyl, pyrimidinyl, pyridinonyl,         piperdinyl, benzimidazole or piperazinyl; each being optionally         independently substituted with one to three C₁₋₄ alkyl,         C₁₋₄alkoxy, hydroxy, nitrile, amino, mono- or di-(C₁₋₃         alkyl)amino, mono- or di-(C₁₋₃ alkylamino)carbonyl, NH₂C(O),         C₁₋₆ alkyl-S(O)_(m) or halogen;     -   Y is:         a bond or a C₁₋₄ saturated or unsaturated branched or unbranched         carbon chain optionally partially or fully halogenated, wherein         one or more C atoms are optionally replaced by O or N, and         wherein Y is optionally independently substituted with one to         two oxo groups, nitrile, phenyl, hydroxy or one or more C₁₋₄         alkyl optionally substituted by one or more halogen atoms;     -   Z is:         phenyl, heteroaryl selected from pyridinyl, imidazolyl, furanyl         and thienyl, heterocycle selected from piperazinyl,         2-oxa-5-aza-bicyclo[2.2.1]heptanyl, pentamethylene sulfidyl,         pentamethylene sulfoxidyl, pentamethylene sulfonyl,         tetrahydrofuranyl, morpholino, thiomorpholino and piperidinyl,         each of the aforementioned Z are optionally substituted with one         to three halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₁₋₃ alkoxy-C₁₋₃         alkyl, C₁₋₆ alkoxycarbonyl, aroyl, morpholinocarbonyl, C₁₋₃acyl,         oxo, hydroxy, pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃ alkyl,         tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl, nitrile,         carboxy, phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino, amino-S(O)_(m), C₁₋₆         alkyl-S(O)_(m) or phenyl-S(O)_(m) wherein the phenyl ring is         optionally substituted with one to two halogen, C₁₋₆ alkoxy,         hydroxy, halogen or mono- or di-(C₁₋₃ alkyl)amino;         or Z is optionally substituted with one to three amino,         aminocarbonyl or amino-C₁₋₃ alkyl wherein the N atom is         optionally independently mono- or di-substituted by         aminoC₁₋₆alkyl, C₁₋₃alkyl, arylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl,         C₁₋₅ alkoxy, aroyl, C₁₋₃acyl, C₁₋₃alkyl-S(O)_(m)— or         arylC₀₋₃alkyl-S(O)_(m)— each of the aforementioned alkyl and         aryl attached to the amino group are optionally substituted with         one to two halogen, C₁₋₆ alkyl or C₁₋₆ alkoxy;         or Z is optionally substituted with one to three aryl,         heterocycle or heteroaryl as hereinabove described in this         paragraph each in turn is optionally substituted by halogen,         C₁₋₆ alkyl or C₁₋₆ alkoxy;         or Z is hydroxy, hydroxyC₁₋₃alkyl, halogen, nitrile, amino         wherein the N atom is optionally independently mono- or         di-substituted by aroyl, C₁₋₃acyl, C₁₋₆alkyl, C₁₋₅ alkoxyC₁₋₃         alkyl, pyridinylC₁₋₃alkyl, tetrahydrafuranylC₁₋₃alkyl,         nitrileC₁₋₄alkyl or phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino,         or Z is C₁₋₆alkyl branched or unbranched, C₁₋₆alkoxy or         nitrileC₁₋₄alkyl;     -   R₁ is:         C₁₋₄ branched or unbranched alkyl optionally partially or fully         halogenated;         cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl         optionally partially or fully halogenated and optionally         substituted with one to three C₁₋₃ alkyl groups, or an 30 analog         of such cycloalkyl group wherein one to three ring methylene         groups are replaced by groups independently selected from the         group consisting of O, S and NH;         C₃₋₁₀ branched alkenyl optionally partially or fully halogenated         and optionally substituted with one to three C₁₋₅ branched or         unbranched alkyl;         cyclopentenyl and cyclohexenyl optionally substituted with one         to three C₁₋₃ alkyl groups;     -   R₂ is:         a C₁₋₆ branched or unbranched alkyl optionally partially or         fully halogenated and optionally substituted with nitrile;     -   R₃ is:         phenyl or heterocyclic group selected from the group consisting         of pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl and pyrazolyl,         wherein such phenyl or heterocyclic group is optionally         substituted with one to five groups selected from the group         consisting of a phenyl, heterocycle selected from the group         hereinabove described in this paragraph, C₁₋₆ branched or         unbranched alkyl which is optionally partially or fully         halogenated, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl,         cycloheptyl, bicyclopentyl, bicyclohexyl, bicycloheptyl, phenyl         C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl, halogen, hydroxy, oxo, nitrile,         C₁₋₃ alkoxy optionally be partially or fully halogenated, C₁₋₃         alkoxyC₁₋₅alkyl, C₁₋₃thioalkyl, C₁₋₃thioalkylC₁₋₅alkyl,         phenyloxy, naphthyloxy, heteraryloxy wherein the heterocyclic         moiety is selected from the group hereinabove described in this         paragraph, nitro, amino, mono- or di-(C₁₋₃)alkylamino,         phenylamino, naphthylamino, heterocyclylamino wherein the         heterocyclyl moiety is selected from the group hereinabove         described in this paragraph, NH₂C(O), a mono- or di-(C₁₋₃)alkyl         aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl, amino-C₁₋₅ alkyl,         mono- or di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, amino-S(O)₂,         di-(C₁₋₃)alkylamino-S(O)₂, R₄—C₁₋₅ alkyl, R₅—C₁₋₅ alkoxy,         R₆—C(O)—C₁₋₅ alkyl and R₇—C₁₋₅ alkyl(R₈)N, carboxy-mono- or         di-(C₁₋₅)-alkyl-amino;         a fused aryl selected from the group consisting of         benzocyclobutanyl, indanyl, indenyl; wherein the fused aryl is         substituted with 0 to 3 groups independently selected from the         group consisting of phenyl, naphthyl and heterocyclyl selected         from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl,         pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl,         isoxazolyl, and isothiazolyl, C₁₋₆ branched or unbranched alkyl         which is optionally partially or fully halogenated, halogen,         nitrile, C₁₋₃ alkoxy which is optionally partially or fully         halogenated, phenyloxy, naphthyloxy, heterocyclyloxy wherein the         heterocyclyl moiety is selected from the group hereinabove         described in this paragraph, nitro, amino, mono- or         di-(C₁₋₃)alkylamino, phenylamino, naphthylamino,         heterocyclylamino wherein the heterocyclyl moiety is selected         from the group hereinabove described in this paragraph, NH₂C(O),         a mono- or di-(C₁₋₃)alkyl aminocarbonyl, C₁₋₄ alkyl-OC(O), C₁₋₅         alkyl-C(O)—C₁₋₄ branched or unbranched alkyl, an amino-C₁₋₅         alkyl, mono- or di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, R₉—C₁₋₅ alkyl,         R₁₀—C₁₋₅ alkoxy, R₁₁—C(O)—C₁₋₅ alkyl and R₁₂—C₁₋₅alkyl(R₁₃)N;         cycloalkyl selected from the group consisting of cyclopropyl,         cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, wherein the         cycloalkyl is optionally partially or fully halogenated and         optionally substituted with one to three C₁₋₃ alkyl groups;         C₁₋₆alkoxycarbonylC₁₋₆alkyl;         or R₁ and R₂ taken together optionally form a fused phenyl or         pyridinyl ring;     -   each R₈ and R₁₃ is independently selected from the group         consisting of: hydrogen and C₁₋₄ branched or unbranched alkyl         optionally partially or fully halogenated; and     -   each R₄, R₅, R₆, R₇, R₉, R₁₀, R₁₁ and R₁₂ is independently         selected from the group consisting of morpholine, piperidine,         piperazine, imidazole and tetrazole;         wherein X is directly attached to one —Y-Z.     -   A yet more preferred subgeneric aspect of the invention         comprises a method of using the compounds of the formula (Ia),         as described in the immediate previous paragraph, wherein:     -   Ar₁ is pyrazole;     -   X is:         cyclopentenyl, cyclohexenyl, cycloheptenyl, optionally         substituted with an oxo group or one to three C₁₋₄ alkyl, C₁₋₄         alkoxy or C₁₋₄ alkylamino chains each being branched or         unbranched;         phenyl, furanyl, thienyl, pyridinyl, pyrazinyl piperidinyl or         pyrimidinyl each being optionally independently substituted with         one to three C₁₋₂ alkyl, C₁₋₂alkoxy, hydroxy or halogen;     -   Z is:         phenyl, heteroaryl selected from pyridinyl, imidazolyl and         furanyl, heterocycle selected from         2-oxa-5-aza-bicyclo[2.2.1]heptanyl, pentamethylene sulfidyl,         pentamethylene sulfoxidyl, pentamethylene sulfonyl,         tetrahydrofuranyl, tetrahydropyranyl, piperazinyl, morpholino,         thiomorpholino, thiomorpholino sulfoxide and piperidinyl, each         of the aforementioned Z are optionally substituted with one to         three halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₁₋₃ alkoxy-C₁₋₃ alkyl,         C₁₋₆ alkoxycarbonyl, aroyl, morpholinocarbonyl, C₁₋₃acyl, oxo,         hydroxy, pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃ alkyl,         tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl, nitrile,         carboxy, phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino, amino-S(O)_(m), C₁₋₆         alkyl-S(O)_(m), or phenyl-S(O)_(m) wherein the phenyl ring is         optionally substituted with one to two halogen, C₁₋₆ alkoxy,         hydroxy, halogen or mono- or di-(C₁₋₃ alkyl)amino;         or Z is optionally substituted with one to three amino,         aminocarbonyl or amino-C₁₋₃ alkyl wherein the N atom is         optionally independently mono- or di-substituted by         aminoC₁₋₆alkyl, C₁₋₃alkyl, arylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl,         C₁₋₅ alkoxy, aroyl, C₁₋₃acyl, C¹⁻³alkyl-S(O)_(m)—,         pyridinylC₀₋₃alkyl, tetrahydrafuranylC₀₋₃alkyl, or         arylC₀₋₃alkyl-S(O)_(m)— each of the aforementioned alkyl and         aryl attached to the amino group is optionally substituted with         one to two halogen, C₁₋₆ alkyl or C₁₋₆ alkoxy;         or Z is hydroxy, hydroxyc₁₋₃alkyl, halogen, nitrile, amino         wherein the N atom is optionally independently mono- or         di-substituted by C₁₋₆alkyl, pyridinylC₀₋₃alkyl,         tetrahydrafuranylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl, C₁₋₃acyl,         nitrileC₁₋₄alkyl or phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino,         or Z is C₁₋₆alkyl branched or unbranched, C₁₋₆alkoxy or         nitrileC₁₋₄alkyl;     -   R₁ is:         C₁₋₄ branched or unbranched alkyl optionally partially or fully         halogenated;         cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl and         cycloheptanyl optionally partially or fully halogenated and         optionally substituted with one to three C₁₋₃ alkyl groups, or         an analog of such cycloalkyl group wherein one to three ring         methylene groups are replaced by groups independently selected         from the group consisting of O, S and NH;         C₃₋₁₀ branched alkenyl optionally partially or fully halogenated         and optionally substituted with one to three C₁₋₃ branched or         unbranched alkyl;         cyclopentenyl and cyclohexenyl optionally substituted with one         to three C₁₋₃ alkyl groups;     -   R₂ is:         a C₁₋₆ branched or unbranched alkyl optionally partially or         fully halogenated and optionally substituted with nitrile;     -   R₃ is:         phenyl or heterocyclic group selected from the group consisting         of pyridinyl, pyrimidinyl, pyridazinyl and pyrazolyl, wherein         such phenyl or heterocyclic group is optionally substituted with         one to five groups selected from the group consisting of a         phenyl, heterocycle selected from the group hereinabove         described in this paragraph, C₁₋₆ branched or unbranched alkyl         which is optionally partially or fully halogenated, phenyl C₁₋₅         alkyl, halogen, hydroxy, oxo, nitrile, C₁₋₃ alkoxy optionally         partially or fully halogenated, C₁₋₃thioalkyl,         C₁₋₃thioalkylC₁₋₅alkyl, amino, mono- or di-(C₁₋₃)alkylamino,         NH₂C(O) or a mono- or di-(C₁₋₃)alkyl aminocarbonyl,         C₁₋₆alkoxycarbonylC₁₋₆alkyl;         or R₃ is cyclopropyl or cyclopentyl each optionally partially or         fully halogenated and optionally substituted with one to three         C₁₋₃ alkyl groups         or R₁ and R₂ taken together optionally form a fused phenyl or         pyridinyl ring.

A yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (Ia), as described in the immediate previous paragraph, and wherein:

-   -   Y is —CH₂—, —O—(CH₂)₀₋₃—, —CH₂CH₂—, —CH₂NH—, —CH₂CH₂—NH—,         NH—CH₂CH₂—, —CH₂—NH—CH₂—, —NH—, —NH—C(O)—, —C(O)—, —CH(OH)—,         —CH₂(CH₂CH₃)— or a bond;     -   X is:         cyclohexenyl optionally substituted with an oxo group or one to         three C₁₋₄ alkyl, C₁₋₄ alkoxy or C₁₋₄ alkylamino chains each         being branched or unbranched;         phenyl, pyridinyl, pyrazinyl, piperidinyl or pyrimidinyl each         being optionally independently substituted with one to three         C₁₋₂ alkyl, C₁₋₂alkoxy, hydroxy or halogen;     -   Z is:         phenyl, heteroaryl selected from pyridinyl, imidazolyl and         furanyl, heterocycle selected from         2-oxa-5-aza-bicyclo[2.2.1]heptanyl, pentamethylene sulfidyl,         pentamethylene sulfoxidyl, pentamethylene sulfonyl,         tetrahydrofuranyl, tetrahydropyranyl, piperazinyl, morpholino,         thiomorpholino, thiomorpholino sulfoxide and piperidinyl, each         of the aforementioned Z are optionally substituted with one to         three halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₁₋₃ alkoxy-C₁₋₃ alkyl,         C₁₋₆ alkoxycarbonyl, aroyl, morpholinocarbonyl, C₁₋₃acyl, oxo,         hydroxy, pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃ alkyl,         tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl, nitrile,         carboxy, phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino, amino-S(O)_(m), C₁₋₆         alkyl-S(O)_(m), or phenyl-S(O)_(m) wherein the phenyl ring is         optionally substituted with one to two halogen, C₁₋₆ alkoxy,         hydroxy, halogen or mono- or di-(C₁₋₃ alkyl)amino;         or Z is optionally substituted with one to three amino or         aminocarbonyl wherein the N atom is optionally independently         mono- or di-substituted by aminoC₁₋₆alkyl, C₁₋₃alkyl,         arylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl, C₁₋₅ alkoxy, aroyl,         C₁₋₃acyl, C₁₋₃alkyl-S(O)_(m)— or arylC₀₋₃alkyl-S(O)_(m)— each of         the aforementioned alkyl and aryl attached to the amino group is         optionally substituted with one to two halogen, C₁₋₆ alkyl or         C₁₋₆ alkoxy;         or Z is hydroxy, hydroxyC₁₋₃alkyl, halogen, nitrile, amino         wherein the N atom is optionally independently mono- or         di-substituted by C₁₋₃alkyl, pyridinylC₁₋₂alkyl,         tetrahydrafuranylC₁₋₂alkyl, C₁₋₃ alkoxyC₁₋₃ alkyl, C₁₋₃acyl,         nitrileC₁₋₄alkyl, phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino,         or Z is C₁₋₆alkyl branched or unbranched, C₁₋₆alkoxy or         nitrileC₁₋₄alkyl;     -   R₁ is:         C₁₋₄ branched or unbranched alkyl optionally partially or fully         halogenated;     -   R₂ is:         a C₁₋₃ branched or unbranched alkyl optionally partially or         fully halogenated and optionally substituted with nitrile;     -   R₃ is:         phenyl or heterocyclic group selected from the group consisting         of pyridinyl, pyrimidinyl, and pyrazolyl, wherein such phenyl or         heterocyclic group is optionally substituted with one to five         groups selected from the group consisting of C₁₋₃ branched or         unbranched alkyl which is optionally partially or fully         halogenated, C₁₋₃ alkoxy which optionally partially or fully         halogenated, C₁₋₃thioalkyl, C₁₋₃thioalkylC₁₋₅alkyl, amino or         NH₂C(O);         C₁₋₃alkoxycarbonyl;         or R₃ is cyclopropyl or cyclopentyl each optionally partially or         fully halogenated and optionally substituted with one to three         C₁₋₃ alkyl groups.

A further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (Ia), as described in the immediate previous paragraph, and wherein:

-   -   Ar₁ is 5-tert-butyl-pyrazol-3-yl; wherein the pyrazole ring is         substituted independently by one to two R₂ or R₃;     -   X is:         cyclohexenyl;         phenyl, pyridinyl, pyrazinyl, piperidinyl or pyrimidinyl each         being optionally independently substituted with C₁₋₂alkoxy or         hydroxy;     -   Z is:         phenyl, heteroaryl selected from pyridinyl and furanyl,         heterocycle selected from 2-oxa-5-aza-bicyclo[2.2.1]heptanyl,         pentamethylene sulfidyl, pentamethylene sulfoxidyl,         tetrahydrofuranyl, piperazinyl, morpholino, thiomorpholino and         piperidinyl, each of the aforementioned Z are optionally         substituted with one to three C₁₋₃ alkyl, C₁₋₃ alkoxy, oxo,         hydroxy or NH₂C(O)—;         or Z is hydroxyc₁₋₃alkyl, amino wherein the N atom is optionally         independently mono- or di-substituted by pyridinylmethyl,         tetrahydrafuranylmethyl, C₁₋₃ alkoxyC₁₋₃ alkyl, C₁₋₃acyl or         nitrileC₁₋₄alkyl,         or Z is nitrileC₁₋₄alkyl;     -   R₃ is:         phenyl or heterocyclic group selected from the group consisting         of pyridinyl, pyrimidinyl, and pyrazolyl, wherein such phenyl or         heterocyclic group is optionally substituted with one to two         groups selected from the group consisting of C₁₋₂ alkyl which is         optionally partially or fully halogenated, C₁₋₂ alkoxy which         optionally partially or fully halogenated, C₁₋₂thioalkyl,         C₁₋₂thioalkylC₁₋₃alkyl, amino or NH₂C(O);         C₁₋₃alkoxycarbonyl;         or R₃ is cyclopropyl or cyclopentyl each optionally partially or         fully halogenated and optionally substituted with one to three         C₁₋₃ alkyl groups.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (Ia), as described in the immediate previous paragraph, and wherein X is pyridinyl.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (Ia), as described in the immediate previous paragraph, and wherein:

the pyridinyl is attached to Ar₁ via the 3-pyridinyl position.

The following compounds are representative of the compounds of formula (Ia) which are useful in the novel methods described herein:

-   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-morpholin-4-yl-methylphenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[3-(4-morpholin-4-yl-methylphenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-morpholin-4-yl-methylfuran-2-yl)-     naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl-methyl)cyclohexenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-(4-morpholin-4-yl)ethylphenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-dimethylaminomethylphenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-(morpholin-4-yl-methyl)pyridin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-     naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-methyl-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-(morpholin-4-yl)ethylamino)cyclohexenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3,4-(morpholin-4-yl-methyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-methylpiperzin-1-yl-methyl)phenyl)-     naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(piperdin-1-yl-methyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-(pyridin-2-yl)ethylamino)cyclohexenyl)-naphthalen-1-yl]-urea;

1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(2-(pyridin-4-yl)ethylaminomethyl)phenyl)naphthalen-1-yl]-urea;

-   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(pyridin-3-yl-methylaminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(3,4-dimethoxyphenylmethyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-oxo-1,6-dihydro-pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)imidazol-1-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)imidazol-1-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(furan-3-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(4-hydroxybutylamino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(pyridin-3-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(4-methyl-3-carbamylphenyl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(imidazol-2-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(3-hydroxymorpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-2-methoxyethy-N-methylaminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(4-hydroxymorpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl-methyl)cyclohexenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(tetrahydrofuran-3-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N,N-di-(2-methoxyethyl)aminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(3-cyanopropoxy)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-morpholin-4-yl-methyl-piperdinyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N,N-di-(2-cyanoethyl)aminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(1-morpholin-4-yl-indan-5-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(furan-2-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(thiomorpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(3-carboxamidomorpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(2-methyl-3-oxo-piperzin-1-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(4-hydroxybutyloxy)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(furan-2-yl-methyl)-3-methoxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(5-(morpholin-4carbonyl)pyrazin-2-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(tetrahydrothiopyran-4-yl-amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-cyanoethyl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(2,6-dimethylmorpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methoxypyridin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-aminoypyridin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-oxo-1,6-dihydropyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-4-carbonyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(2-oxa-5-aza-bicyclo[2.2.1]hept-5-yl-methyl)pyridin-3-yl)-     naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(3-carbamylphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-(2-cyanoethyl)-N-(pyridin-3-yl-methyl)aminomethyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-(2-cyanoethyl)-N-(pyridin-2-yl-methyl)aminomethyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-(2-cyanoethyl)-N-(tetrahydrofuran-2-yl-methyl)aminomethyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)-4-methoxypyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-morpholin-4-yl-propyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(N-(3-methoxypropyl)amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(N-(3-methoxypropyl)-N-methylamino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-methyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-benzyl-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-N-di-(2-cyanoethyl)aminomethyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(4-carbamylphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-tetrahydrothiopyran-4yl-amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(tetrahydropyran-4yl-amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-(3-cyanopropyl)-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-methanesulfinylphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-methanesulfonylphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-sulfonamidophenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl)carbonylphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(5-(tetrahydrothiopyran-4yl-amino)pyrazin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(methylcarbonylamino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-4-carbonyl)phenyl)     -naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-(3-methylsulfanylpropyl)-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-(morpholin-4-yl-carbonyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(5-(morpholin-4-yl-methyl)pyrazin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-aminopyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-methylpiperdin-4-yl-amino)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(2-methyl-3-oxo-piperzin-1-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-carbonyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(N,N-di-(2-methoxyethyl)aminomethyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-thiomorpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(tetrahydropyran-4-yl-amino)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(5-(morpholin-4-yl-methyl)pyrazin-2-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylthiopyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(2-methyl-3-oxo-piperzin-1-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(pyridin-3-yl-oxy)pyridin-3-yl)naphthalen-1-yl]-urea -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(pyridin-3-yl-amino)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methoxypyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-carbamylpyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-aminopyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-methyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-cyclopropylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-(pyridin-3-yl-amino)pyrimidin-5-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-tetrahydrothiopyran-4-yl-     amino)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(thiomorpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-benzyl-3H-imidazo[4,5-b]pyridin-6-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(pyridin-3-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-(morpholin-4-yl-carbonyl)pyrimidin-5-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-(morpholin-4-yl-methyl)pyrimidin-5-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(3-amino-4-carbamylphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-thiomorpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(pyridin-3-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(hydroxy-pyridin-3-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(2-(morpholin-4-yl-methyl)pyrimidin-5-yl)naphthalen-1-yl]-urea;     and the pharmaceutically acceptable derivatives thereof.

In another embodiment of the invention there are provided the following compounds of formula (Ia) which are useful in the novel methods described herein:

-   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(5-(morpholin-4-yl-methyl)pyridin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(2-(pyridin-2-yl)ethylamino)cyclohexenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(4-(pyridin-3-yl-methylaminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(4-hydroxybutylamino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(4-methyl-3-carbamylphenyl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(3-hydroxypiperidin-1-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(4-hydroxymorpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(3-(morpholin-4-yl-methyl)cyclohexenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(tetrahydrofuran-3-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N,N-di-(2-methoxyethyl)aminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(3-cyanopropoxy)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-morpholin-4-yl-methyl-piperdinyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N,N-di-(2-45     cyanoethyl)aminomethyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(furan-2-yl-methyl)-3-hydroxyphenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(thiomorpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(3-carboxamidopiperidin-1-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(2-methyl-3-oxo-piperzin-1-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(4-hydroxybutyloxy)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(tetrahydrothiopyran-4-yl-amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-cyanoethyl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(2,6-dimethylmorpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methoxypyridin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-aminoypyridin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-4-carbonyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(2-oxa-5-aza-bicyclo[2.2.1]hept-5-yl-methyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-(2-cyanoethyl)     -N-(pyridin-3-yl-methyl)aminomethyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(4-(N-(2-cyanoethyl)-N-(tetrahydrofuran-2-yl-methyl)aminomethyl)phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)-4-methoxypyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-morpholin-4-yl-propyl)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-methyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-tetrahydrothiopyran-4yl-amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(tetrahydropyran-4yl-amino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(5-(tetrahydrothiopyran-4yl-amino)pyrazin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(6-methyl-pyridin-3-yl)-2H-pyrazol-3-yl]-3-[4-(6-(methylcarbonylamino)pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-(3-methylsulfanylpropyl)-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-thiomorpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(tetrahydropyran-4-yl-amino)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylthiopyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-aminopyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(6-(morpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[3-tert-butyl-1′-methyl-1′H-[1,4′]bipyrazol-5-yl]-3-[4-(6-(morpholin-4-yl-methyl)phenyl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-tetrahydrothiopyran-4-yl-amino)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(thiomorpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-(morpholin-4-yl-carbonyl)pyrimidin-5-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(2-(morpholin-4-yl-methyl)pyrimidin-5-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl]-3-[4-(6-(1-oxo-thiomorpholin-4-yl-methyl)pyridin-3-yl)naphthalen-1-yl]-urea; -   1-[5-tert-butyl-2-(2-methylpyrimidin-5-yl)-2H-pyrazol-3-yl]-3-[4-(2-(morpholin-4-yl-methyl)pyrimidin-5-yl)naphthalen-1-yl]-urea     and     the pharmaceutically acceptable derivatives thereof.

In a third broad generic aspect, there is provided a method of treating a cytokine mediated disease or condition chosen from: acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the formula (II) disclosed in WO 00/55139 which is the PCT case of U.S. application Ser. No. 09/505,582:

-   -   wherein:     -   G is:         an aromatic C₆₋₁₀ carbocycle or a nonaromatic C₃₋₁₀ carbocycle         saturated or unsaturated;         a 6-10 membered heteroaryl containing 1 or more heteroatoms         chosen from O, N and S;         a 5-8 membered monocyclic heterocycle containing one or more         heteroatoms chosen from O, N and S;         or         an 8-11 membered bicyclic heterocycle, containing one or more         heteroatoms chosen from O, N and S;         wherein G is substituted by one or more R₁, R₂ or R₃;     -   Ar is:         phenyl, naphthyl, quinolinyl, isoquinolinyl, tetrahydronaphthyl,         tetrahydroquinolinyl, tetrahydroisoquinolinyl, benzimidazolyl,         benzofuranyl, dihydrobenzofuranyl, indolinyl, benzothienyl,         dihydrobenzothienyl, indanyl, indenyl or indolyl each being         optionally substituted by one or more R₄ or R₅;     -   X is:         a C₅₋₈ cycloalkyl or cycloalkenyl optionally substituted with         one to two oxo groups or one to three C₁₋₄ alkyl, C₁₋₄ alkoxy or         C₁₋₄ alkylamino chains;         phenyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl,         pyridinyl, pyrimidinyl, pyridinonyl, dihydropyridinonyl,         maleimidyl, dihydromaleimidyl, piperdinyl, benzimidazole,         3H-imidazo[4,5-b]pyridine, piperazinyl, pyridazinyl or         pyrazinyl;     -   Y is:         a bond or a C₁₋₄ saturated or unsaturated branched or unbranched         carbon chain optionally partially or fully halogenated, wherein         one or more methylene groups are optionally replaced by O, N, or         S(O)_(m) and wherein Y is optionally independently substituted         with one to two oxo groups, phenyl or one or more C₁₋₄ alkyl         optionally substituted by one or more halogen atoms;     -   Z is:         phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl,         imidazolyl, pyrazolyl, triazolyl, tetrazolyl, furanyl, thienyl,         pyranyl each being optionally substituted with one to three         halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, hydroxy, amino, mono- or         di-(C₁₋₃ alkyl)amino, C₁₋₆ alkyl-S(O)_(m), CN, CONH₂, COOH or         phenylamino wherein the phenyl ring is optionally substituted         with one to two halogen, C₁₋₆ alkyl or C₁₋₆ alkoxy;         tetrahydropyranyl, tetrahydrofuranyl, 1,3-dioxolanonyl,         1,3-dioxanonyl, 1,4-dioxanyl, morpholinyl, thiomorpholinyl,         thiomorpholino sulfoxidyl, thiomorpholino sulfonyl, piperidinyl,         piperidinonyl, piperazinyl, tetrahydropyrimidonyl,         cyclohexanonyl, cyclohexanolyl, pentamethylene sulfidyl,         pentamethylene sulfoxidyl, pentamethylene sulfonyl,         tetramethylene sulfide, tetramethylene sulfoxidyl or         tetramethylene sulfonyl each being optionally substituted with         one to three nitrile, C₁₋₆ alkyl, C₁₋₆ alkoxy, hydroxy, amino,         mono- or di-(C₁₋₃ alkyl)amino-C₁₋₃ alkyl, CONH₂,         phenylamino-C₁₋₃ alkyl or C₁₋₃ alkoxy-C₁₋₃ alkyl;         halogen, C₁₋₄ alkyl, nitrile, amino, hydroxy, C₁₋₆ alkoxy,         NH₂C(O), mono- or di(C₁₋₃alkyl) aminocarbonyl, mono- or di(C₁₋₆         alkyl)amino, secondary or tertiary amine wherein the amino         nitrogen is covalently bonded to C₁₋₃ alkyl or C₁₋₅ alkoxyalkyl,         pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃ alkyl,         tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl,         carboxamide-C₁₋₃ alkyl, phenyl, wherein the phenyl ring is         optionally substituted with one to two halogen, C₁₋₆ alkoxy,         hydroxy or mono- or di-(C₁₋₃ alkyl)amino, C₁₋₆ alkyl-S(O)_(m),         or phenyl-S(O)_(m), wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy,         halogen or mono- or di-(C₁₋₃ alkyl)amino;         C₁₋₆ alkyl-S(O)_(m), and phenyl-S(O)_(m), wherein the phenyl         ring is optionally substituted with one to two halogen, C₁₋₆         alkoxy, hydroxy or mono- or di-(C₁₋₃ alkyl)amino;     -   each R₁ is independently:         C₁₋₁₀ alkyl optionally be partially or fully halogenated, and         optionally substituted with one to three C₃₋₁₀ cycloalkanyl,         hydroxy, phenyl, naphthyl, pyridinyl, pyrimidinyl, pyrazinyl,         pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl,         isoxazolyl or isothiazolyl; each of the aforementioned being         optionally substituted with one to five groups selected from         halogen, C₁₋₆ alkyl which is optionally partially or fully         halogenated, C₃₋₈ cycloalkanyl, C₅₋₈ cycloalkenyl, hydroxy,         nitrile, C₁₋₃ alkoxy which is optionally partially or fully         halogenated or NH₂C(O), mono- or di(C₁₋₃alkyl)amino, and mono-         or di(C₁₋₃alkyl)aminocarbonyl;         cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, or         cycloheptyloxy each being optionally partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups optionally partially or fully halogenated, CN,         hydroxyC₁₋₃alkyl or aryl;         or an analog of such cycloalkyl group wherein one to three ring         methylene groups are independently replaced by O, S(O)_(m),         CHOH, >C═O, >C═S or NH;         phenyloxy or benzyloxy each being optionally partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups optionally partially or fully halogenated, CN,         hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloaryl group         wherein one to two ring methyne groups are independently         replaced by N;         cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl,         cycloheptanyl, bicyclopentanyl, bicyclohexanyl or         bicycloheptanyl, each being optionally partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups optionally partially or fully halogenated, CN,         hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloalkyl group         wherein one to three ring methylene groups are independently         replaced by O, S(O)_(m), CHOH, >C═O, >C═S or NH;         C₃₋₁₀ branched or unbranced alkenyl each being optionally         partially or fully halogenated, and optionally be substituted         with one to three C₁₋₅ branched or unbranched alkyl, phenyl,         naphthyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl,         pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl or         isothiazolyl, each of the aforementioned being substituted with         zero to five halogen, C₁₋₆ alkyl which is optionally partially         or fully halogenated, cyclopropanyl, cyclobutanyl,         cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl,         bicyclohexanyl and bicycloheptanyl, hydroxy, nitrile, C₁₋₃         alkyloxy which is optionally partially or fully halogenated,         NH₂C(O), mono- or di(C₁₋₃alkyl)aminocarbonyl; the C₃₋₁₀ branched         or unbranced alkenyl being optionally interrupted by one or more         heteroatoms chosen from O, N and S(O)_(m);         cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,         cycloheptadienyl, bicyclohexenyl or bicycloheptenyl, wherein         such cycloalkenyl group is optionally substituted with one to         three C₁₋₃ alkyl groups;         nitrile, halogen;         methoxycarbonyl, ethoxycarbonyl and propoxycarbonyl;         silyl containing three C₁₋₄ alkyl groups optionally partially or         fully halogenated;         C₃₋₆ alkynyl branched or unbranched carbon chain optionally         partially or fully halogenated, wherein one or more methylene         groups are optionally replaced by O, NH or S(O)_(m) and wherein         said alkynyl group is optionally independently substituted with         one to two oxo groups, pyrrolidinyl, pyrrolyl, one or more C₁₋₄         alkyl optionally substituted by one or more halogen atoms,         nitrile, morpholino, piperidinyl, piperazinyl, imidazolyl,         phenyl, pyridinyl, tetrazolyl, or mono- or di(C₁₋₃ alkyl)amino         optionally substituted by one or more halogen atoms;         each R₂, R₄, and R₅ is         a C₁₋₆ branched or unbranched alkyl optionally partially or         fully halogenated, acetyl, aroyl, C₁₋₄ branched or unbranched         alkoxy, each being optionally partially or fully halogenated,         halogen, nitrile, methoxycarbonyl, C₁₋₃ alkyl-S(O)_(m)         optionally partially or fully halogenated, or phenylsulfonyl;         C₁₋₆ alkoxy, hydroxy, amino, or mono- or di-(C₁₋₄ alkyl)amino,         nitrile, halogen;         OR₆;         nitro; or         mono- or di-(C₁₋₄ alkyl)amino-S(O)₂ optionally partially or         fully halogenated, or H₂NSO₂;     -   each R₃ is independently:         phenyl, naphthyl, morpholinyl, pyridinyl, pyrimidinyl,         pyrazinyl, pyridazinyl, pyrrolyl, pyrrolidinyl, imidazolyl,         pyrazolyl, thiazolyl, oxazoyl, triazolyl, tetrazolyl, thienyl,         furyl, tetrahydrofuryl, isoxazolyl, isothiazolyl, quinolinyl,         isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl,         benzoxazolyl, benzisoxazolyl, benzpyrazolyl, benzothiofuranyl,         cinnolinyl, pterindinyl, phthalazinyl, naphthypyridinyl,         quinoxalinyl, quinazolinyl, purinyl or indazolyl, each of the         aforementioned is optionally substituted with one to three         phenyl, naphthyl, heterocycle or heteroaryl as hereinabove         described in this paragraph, C₁₋₆ branched or unbranched alkyl         which is optionally partially or fully halogenated,         cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl,         cycloheptanyl, bicyclopentanyl, bicyclohexanyl, bicycloheptanyl,         phenyl C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl, halogen, hydroxy, oxo,         nitrile, C₁₋₃ alkyloxy optionally partially or fully         halogenated, phenyloxy, naphthyloxy, heteroaryloxy or         heterocyclicoxy wherein the heterocyclic or heteroaryl moiety is         as hereinabove described in this paragraph, nitro, amino, mono-         or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl         or heterocyclic amino wherein the heteroaryl heterocyclic moiety         is as hereinabove described in this paragraph, NH₂C(O), a mono-         or di-(C₁₋₃alkyl) aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl,         amino-C₁₋₅ alkyl, mono- or di-(C₁₋₃alkyl)amino-C₁₋₅ alkyl,         amino-S(O)₂, di-(C₁₋₃alkyl)amino-S(O)₂, R₇—C₁₋₅ alkyl, R₈—C₁₋₅         alkoxy, R₉—C(O)—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkyl(R₁₁)N, carboxy-mono-         or di-(C₁₋₅alkyl)-amino;         a fused aryl selected from benzocyclobutanyl, indanyl, indenyl,         dihydronaphthyl, tetrahydronaphthyl, benzocycloheptanyl and         benzocycloheptenyl, or a fused heteroaryl selected from         cyclopentenopyridinyl, cyclohexanopyridinyl,         cyclopentanopyrimidinyl, cyclohexanopyrimidinyl,         cyclopentanopyrazinyl, cyclohexanopyrazinyl,         cyclopentanopyridazinyl, cyclohexanopyridazinyl,         cyclopentanoquinolinyl, cyclohexanoquinolinyl,         cyclopentanoisoquinolinyl, cyclohexanoisoquinolinyl,         cyclopentanoindolyl, cyclohexanoindolyl,         cyclopentanobenzimidazolyl, cyclohexanobenzimidazolyl,         cyclopentanobenzoxazolyl, cyclohexanobenzoxazolyl,         cyclopentanoimidazolyl, cyclohexanoimidazolyl,         cyclopentanothienyl and cyclohexanothienyl; wherein the fused         aryl or fused heteroaryl ring is independently substituted with         zero to three phenyl, naphthyl, pyridinyl, pyrimidinyl,         pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl,         thienyl, furyl, isoxazolyl, isothiazolyl, C₁₋₆ alkyl which is         optionally partially or fully halogenated, halogen, nitrile,         C₁₋₃ alkyloxy which is optionally partially or fully         halogenated, phenyloxy, naphthyloxy, heteroaryloxy or         heterocyclicoxy wherein the heteroaryl or heterocyclic moiety is         as hereinabove described in this paragraph, nitro, amino, mono-         or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl         or heterocyclic amino wherein the heteroaryl or heterocyclic         moiety is as hereinabove described in this paragraph, NH₂C(O),         mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₄ alkyl-OC(O), C₁₋₅         alkyl-C(O)—C₁₋₄ alkyl, amino-C₁₋₅ alkyl, mono- or         di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, R₁₂—C₁₋₅ alkyl, R₁₃—C₁₋₅ alkoxy,         R₁₄—C(O)—C₁₋₅ alkyl or R₁₅—C₁₋₅ alkyl(R₁₆)N;         cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl,         cycloheptanyl, bicyclopentanyl, bicyclohexanyl or         bicycloheptanyl, each being optionally partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups, or an analog of such cycloalkyl group wherein one         to three ring methylene groups are independently replaced by O,         S, CHOH, >C═O, >C═S or NH;         cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,         cycloheptadienyl, bicyclohexenyl or bicycloheptenyl, each         optionally substituted with one to three C₁₋₃ alkyl groups;         C₁₋₄ alkyl-phenyl-C(O)—C₁₋₄ alkyl-, C₁₋₄ alkyl-C(O)—C₁₋₄ alkyl-         or C₁₋₄ alkyl-phenyl-S(O)_(m)—C₁₋₄ alkyl-;         C₁₋₆ alkyl or C₁₋₆ branched or unbranched alkoxy each of which         is optionally partially or fully halogenated or optionally         substituted with R₁₇;         OR₁₈ or C₁₋₆ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₅alkyl)amino optionally substituted         with R₁₉;         R₂₀C(O)N(R₂₁)—, R₂₂O— or R₂₃R₂₄NC(O)—; R₂₆(CH₂)_(m)C(O)N(R₂₁)—         or R₂₆C(O)(CH₂)_(m)N(R₂₁)—; —C₂₋₆alkenyl substituted by         R₂₃R₂₄NC(O)—;         C₂₋₆ alkynyl branched or unbranched carbon chain, optionally         partially or fully halogenated, wherein one or more methylene         groups are optionally replaced by O, NH, S(O)_(m) and wherein         said alkynyl group is optionally independently substituted with         one to two oxo groups, pyrroldinyl, pyrrolyl, morpholinyl,         piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl,         tetrazolyl one or more C₁₋₄ alkyl optionally substituted by one         or more halogen atoms, nitrile, morpholino, piperidinyl,         piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono-         or di(C₁₋₄ alkyl)amino optionally substituted by one or more         halogen atoms; or         aroyl;     -   R₆ is a:         C₁₋₄ alkyl optionally partially or fully halogenated and         optionally substituted with R₂₆;     -   each R₇, R₈, R₉, R₁₀, R₁₂, R₁₃, R₁₄, R₁₅, R₁₇, R₁₉, R₂₅ and R₂₆         is independently: nitrile, phenyl, morpholino, piperidinyl,         piperazinyl, imidazolyl, pyridinyl, tetrazolyl, amino or mono-         or di-(C₁₋₄alkyl)amino optionally partially or fully         halogenated;     -   each R₁₁ and R₁₆ is independently:         hydrogen or C₁₋₄ alkyl optionally partially or fully         halogenated;     -   R₁₈ is independently:         hydrogen or a C₁₋₄ alkyl optionally independently substituted         with oxo or R₂₅;     -   R₂₀ is independently:         C₁₋₁₀ alkyl optionally partially or fully halogenated, phenyl,         or pyridinyl;     -   R₂₁ is independently:         hydrogen or C₁₋₃ alkyl optionally partially or fully         halogenated;     -   each R₂₂, R₂₃ and R₂₄ is independently:         hydrogen, C₁₋₆ alkyl optionally partially or fully halogenated,         said C₁₋₆ alkyl is optionally interrupted by one or more O, N or         S, said C₁₋₆ alkyl also being independently optionally         substituted by mono- or di-(C₁₋₃alkyl)aminocarbonyl, phenyl,         pyridinyl, amino or mono- or di-(C₁₋₄alkyl)amino each of which         is optionally partially or fully halogenated and optionally         substituted with mono- or di-(C₁₋₃alkyl)amino;         or R₂₃ and R₂₄ taken together optionally form a heterocyclic or         heteroaryl ring;

-   m=0, 1 or 2;

-   W is O or S and     the pharmaceutically acceptable derivatives thereof.

A preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II) as provided above and wherein:

G is:

phenyl, naphthyl, benzocyclobutanyl, dihydronaphthyl, tetrahydronaphthyl, benzocycloheptanyl, benzocycloheptenyl, indanyl, indenyl;

pyridinyl, pyridonyl, quinolinyl, dihydroquinolinyl, tetrahydroquinoyl, isoquinolinyl, tetrahydroisoquinoyl, pyridazinyl, pyrimidinyl, pyrazinyl, benzimidazolyl, benzthiazolyl, benzoxazolyl, benzofuranyl, benzothiophenyl, benzpyrazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, benzooxazolonyl, benzo[1,4]oxazin-3-onyl, benzodioxolyl, benzo[1,3]dioxol-2-onyl, benzofuran-3-onyl, tetrahydrobenzopyranyl, indolyl, indolinyl, indolonyl, indolinonyl, phthalimidyl;

oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, piperidinyl, piperazinyl, morpholinyl, tetrahydropyranyl, dioxanyl, tetramethylene sulfonyl, tetramethylene sulfoxidyl, oxazolinyl, thiazolinyl, imidazolinyl, tertrahydropyridinyl, homopiperidinyl, pyrrolinyl, tetrahydropyrimidinyl, decahydroquinolinyl, decahydroisoquinolinyl, thiomorpholinyl, thiazolidinyl, dihydrooxazinyl, dihydropyranyl, oxocanyl, heptacanyl, thioxanyl or dithianyl;

wherein G is substituted by one or more R₁, R₂ or R₃;

A more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II) as provided above and wherein:

G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl, isoquinolinyl, pyrazinyl, benzimidazolyl, benzoxazolyl, benzofuranyl, benzothiophenyl, benzpyrazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, indanyl, indenyl, indolyl, indolinyl, indolonyl or indolinonyl, wherein G is substituted by one or more R₁, R₂ or R₃;

-   -   Ar is:         naphthyl, quinolinyl, isoquinolinyl, tetrahydronaphthyl,         tetrahydroquinolinyl, tetrahydroisoquinolinyl, indanyl, indenyl         or indolyl each being optionally substituted by one or more R₄         or R₅ groups;     -   X is:         phenyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl,         pyridinyl, pyrimidinyl, pyridinonyl, dihydropyridinonyl,         maleimidyl, dihydromaleimidyl, piperdinyl, piperazinyl,         pyridazinyl or pyrazinyl     -   Y is:         a bond or         a C₁₋₄ saturated or unsaturated carbon chain wherein one of the         carbon atoms is optionally replaced by O, N, or S(O)_(m) and         wherein Y is optionally independently substituted with one to         two oxo groups, phenyl or one or more C₁₋₄ alkyl optionally         substituted by one or more halogen atoms;     -   Z is:         phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl,         imidazolyl, furanyl, thienyl, dihydrothiazolyl, dihydrothiazolyl         sulfoxidyl, pyranyl, pyrrolidinyl which are optionally         substituted with one to three nitrile, C₁₋₃ alkyl, C₁₋₃ alkoxy,         amino, mono- or di-(C₁₋₃ alkyl)amino, CONH₂ or OH;         tetrahydropyranyl, tetrahydrofuranyl, 1,3-dioxolanonyl,         1,3-dioxanonyl, 1,4-dioxanyl, morpholinyl, thiomorpholinyl,         thiomorpholino sulfoxidyl, piperidinyl, piperidinonyl,         piperazinyl, tetrahydropyrimidonyl, pentamethylene sulfidyl,         pentamethylene sulfoxidyl, pentamethylene sulfonyl,         tetramethylene sulfidyl, tetramethylene sulfoxidyl or         tetramethylene sulfonyl which are optionally substituted with         one to three nitrile, C₁₋₃ alkyl, C₁₋₃ alkoxy, amino, mono- or         di-(C₁₋₃ alkyl)amino, CONH₂, or OH; nitrile, C₁₋₆         alkyl-S(O)_(m), halogen, hydroxy, C₁₋₄ alkoxy, amino, mono- or         di-(C₁₋₆ alkyl)amino, mono- or di-(C₁₋₃ alkyl)aminocarbonyl or         NH₂C(O);     -   each R₁ is independently:         C₃₋₆ alkyl optionally partially or fully halogenated, and         optionally substituted with one to three C₃₋₆cycloalkyl, phenyl,         thienyl, furyl, isoxazolyl or isothiazolyl; each of the         aforementioned being optionally substituted with one to three         groups selected from halogen, C₁₋₃ alkyl which is optionally         partially or fully halogenated, hydroxy, nitrile or C₁₋₃alkoxy         which is optionally partially or fully halogenated;         cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl,         bicyclopentanyl or bicyclohexanyl, each being optionally         partially or fully halogenated and optionally substituted with         one to three C₁₋₃ alkyl groups optionally partially or fully         halogenated, CN, hydroxyC₁₋₃alkyl or phenyl; or an analog of         such cycloalkyl group wherein one to three ring methylene groups         are independently replaced by O, S, CHOH, >C═O, >C═S or NH; or         silyl containing three C₁₋₄ alkyl groups optionally partially or         fully halogenated;     -   R₂ is independently:         halogen, C₁₋₃ alkoxy, C₁₋₃ alkyl-S(O)_(m) optionally partially         or fully halogenated, phenylsulfonyl or nitrile;     -   R₃ is independently:         phenyl, morpholino, pyridinyl, pyrimidinyl, pyrazinyl, pyrrolyl,         pyrrolylidinyl, imidazolyl, pyrazolyl, each being optionally         substituted with one to three phenyl, naphthyl, heterocycle or         heteroaryl as hereinabove described in this paragraph, C₁₋₆         alkyl which is optionally partially or fully halogenated,         cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl,         cycloheptanyl, bicyclopentanyl, bicyclohexanyl, bicycloheptanyl,         phenyl C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl, halogen, oxo, hydroxy,         nitrile, C₁₋₃ alkyloxy optionally partially or fully         halogenated, phenyloxy, naphthyloxy, heteroaryloxy or         heterocyclicoxy wherein the heteroaryl or heterocyclic moiety is         as hereinabove described in this paragraph, nitro, amino, mono-         or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl         or heterocyclic amino wherein the heteroaryl or heterocyclic         moiety is as hereinabove described in this paragraph, NH₂C(O), a         mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄         alkyl, mono- or di-(C₁₋₃alkyl)amino, mono- or         di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, mono- or         di-(C₁₋₃alkyl)amino-S(O)₂, R₇—C₁₋₅ alkyl, R₈—C₁₋₅ alkoxy,         R₉—C(O)—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkyl(R₁₁)N, carboxy-mono- or         di-(C₁₋₅)-alkyl-amino;         C₁₋₃ alkyl or C₁₋₄ alkoxy each being optionally partially or         fully halogenated or optionally substituted with R₁₇;         OR₁₈ or C₁₋₆ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₅ alkyl)amino optionally substituted         with R₁₉;         R₂₀C(O)N(R₂₁)—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)— or         R₂₆C(O)CH₂N(R₂₁)—; C₂₋₄alkenyl substituted by R₂₃R₂₄NC(O)—; or         C₂₋₄ alkynyl branched or unbranched carbon chain optionally         partially or fully halogenated and optionally independently         substituted with one to two oxo groups, pyrroldinyl, pyrrolyl,         morpholinyl, piperidinyl, piperazinyl, imidazolyl, phenyl,         pyridinyl, tetrazolyl or one or more C₁₋₄ alkyl optionally         substituted by one or more halogen atoms; and         R₂₃ and R₂₄ taken together optionally form imidazolyl,         piperidinyl, morpholinyl, piperazinyl or a pyridinyl ring.

A yet more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II), as described in the immediate previous paragraph, wherein:

G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl, isoquinolinyl, pyrazinyl, benzothiophenyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, indanyl, indolyl, indolinyl, indolonyl or indolinonyl, wherein G is substituted by one or more R₁, R₂ or R₃;

-   -   Ar is naphthyl;     -   X is         phenyl, imidazolyl, pyridinyl, pyrimidinyl, piperdinyl,         piperazinyl, pyridazinyl or pyrazinyl each being optionally         independently substituted with one to three C₁₋₄ alkyl,         C₁₋₄alkoxy, hydroxy, nitrile, amino, mono- or di-(C₁₋₃         alkyl)amino, mono- or di-(C₁₋₃ alkylamino)carbonyl, NH₂C(O),         C₁₋₆ alkyl-S(O)_(m) or halogen;     -   Y is:         a bond or         a C₁₋₄ saturated carbon chain wherein one of the carbon atoms is         optionally replaced by O, N or S and wherein Y is optionally         independently substituted with an oxo group;     -   Z is:         phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl,         imidazolyl, dihydrothiazolyl, dihydrothiazolyl sulfoxide,         pyranyl or pyrrolidinyl which are optionally substituted with         one to two C₁₋₂ alkyl or C₁₋₂ alkoxy;         tetrahydropyranyl, morpholinyl, thiomorpholinyl, thiomorpholino         sulfoxidyl, piperidinyl, piperidinonyl, piperazinyl or         tetrahydropyrimidonyl which are optionally substituted with one         to two C₁₋₂ alkyl or C₁₋₂ alkoxy; or         C₁₋₃ alkoxy;     -   each R₁ is independently:         C₃₋₅ alkyl optionally partially or fully halogenated, and         optionally substituted with phenyl substituted with zero to         three halogen, C₁₋₃ alkyl which is optionally partially or fully         halogenated, hydroxy, nitrile or C₁₋₃alkoxy which is optionally         partially or fully halogenated;         cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl,         bicyclopentanyl or bicyclohexanyl, each being optionally         partially or fully halogenated and optionally substituted with         one to three C₁₋₃ alkyl groups optionally partially or fully         halogenated, CN, hydroxyC₁₋₃alkyl or phenyl; and an analog of         cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl,         bicyclopentanyl or bicyclohexanyl wherein one ring methylene         group is replaced by O; and         silyl containing three C₁₋₂ independently alkyl groups         optionally partially or fully halogenated;     -   each R₂ is independently:         bromo, chloro, fluoro, methoxy, methylsulfonyl or nitrile;     -   each R₃ is independently:         phenyl, morpholino, pyridinyl, pyrimidinyl, pyrrolylidinyl,         2,5-pyrrolidin-dionyl, imidazolyl, pyrazolyl, each of the         aforementioned is optionally substituted with one to three C₁₋₃         alkyl which is optionally partially or fully halogenated,         halogen, oxo, hydroxy, nitrile and C₁₋₃ alkyloxy optionally         partially or fully halogenated;         C₁₋₃ alkyl or C₁₋₃ alkoxy each being optionally partially or         fully halogenated or optionally substituted with R₁₇;         OR₁₈ or C₁₋₃ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₃ alkyl)amino optionally substituted         with R₁₉;         R₂₀C(O)N(R₂₁)—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)— or         R₂₆C(O)CH₂N(R₂₁)—;         C₂₋₄ alkenyl substituted by R₂₃R₂₄NC(O)—; or         C₂₋₄ alkynyl substituted with pyrroldinyl or pyrrolyl; and         R₂₃ and R₂₄ taken together optionally form morpholino.

A yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II), as described in the immediate previous paragraph, and wherein:

G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl, isoquinolinyl, dihydrobenzofuranyl, indanyl, indolinyl, indolonyl, or indolinonyl, wherein G is substituted by one or more R₁, R₂ or R₃;

-   -   Ar is 1-naphthyl;     -   X is:         phenyl, imidazolyl, pyridinyl, pyrimidinyl, piperdinyl,         piperazinyl, pyridazinyl or pyrazinyl;     -   Y is:         a bond or —CH₂—, —CH₂CH₂—, —C(O)—, —O—, —S—, —NH—CH₂CH₂CH₂—,         —N(CH₃)—, or —NH—;     -   each R₁ is independently:         C₃₋₅ alkyl optionally partially or fully halogenated, and         optionally substituted with phenyl;         cyclopropyl, cyclopentanyl, cyclohexanyl and bicyclopentanyl         optionally substituted with one to three methyl groups         optionally partially or fully halogenated, CN, hydroxymethyl or         phenyl; or 2-tetrahydrofuranyl substituted by methyl; or         trimethyl silyl;     -   each R₃ is independently:         phenyl, morpholinyl, pyridinyl, pyrimidinyl, pyrrolylidinyl,         2,5-pyrrolidin-dionyl, imidazolyl or pyrazolyl, wherein any of         the aforementioned is optionally substituted with C₁₋₂ alkyl         which is optionally partially or fully halogenated;         C₁₋₃ alkyl or C₁₋₃ alkoxy each being optionally partially or         fully halogenated or optionally substituted with diethylamino;         OR₁₈ or C₁₋₃ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₃ alkyl)amino optionally substituted         with R₁₉;         CH₃C(O)NH—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)— or         R₂₆C(O)CH₂N(R₂₁)—;         C₂₋₄alkenyl substituted by R₂₃R₂₄NC(O)—; or         C₂₋₄ alkynyl substituted with pyrroldinyl or pyrrolyl;         R₂₃ and R₂₄ are H or R₂₃ and R₂₄ taken together optionally form         morpholino; and         R₂₆ is morpholino.

A further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II), as described in the immediate previous paragraph, and wherein:

-   -   G is         phenyl, pyridinyl or naphthyl wherein G is substituted by one or         more R₁, R₂ or R₃;     -   X is:         imidazolyl or pyridinyl;     -   Y is:         —CH₂₋, —NH—CH₂CH₂CH₂— or —NH—;     -   Z is morpholino;     -   each R₁ is independently:         tert-butyl, sec-butyl, tert-amyl or phenyl;     -   R₂ is chloro;     -   R₃ is independently:         methyl, methoxy, methoxymethyl, hydroxypropyl, acetamide,         morpholino or morpholinocarbonyl.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II), as described in the immediate previous paragraph, and wherein X is pyridinyl.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (II), as described immediately above, and wherein the pyridinyl is attached to Ar via the 3-pyridinyl position.

The following compounds are representative of the compounds of formula (II) which are useful in the novel methods described herein:

-   1-(3-Cyano-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Fluoro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Chloro-2-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Chloro-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3,4-Dimethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Iodo-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-m-tolyl-urea; -   1-(4-Methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Chloro-4-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Chloro-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,5-Dichloro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-naphthalen-2-yl-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-phenyl-urea; -   1-(3-Chloro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Chloro-3-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(2,4,6-trichloro-phenyl)-urea; -   1-(2-Methyl-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methyl-2-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,3-Dichloro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methoxy-5-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Chloro-6-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,4-Dichloro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methyl-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,4-Dimethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,3-Dimethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Cyano-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3,4,5-trimethoxy-phenyl)-urea; -   1-Biphenyl-4-yl-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,5-Difluoro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Chloro-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Fluoro-3-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Benzyloxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Fluoro-6-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Fluoro-3-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(2,4,5-trimethyl-phenyl)-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(4-trifluoromethyl-phenyl)-urea; -   1-(3-Methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Fluoro-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methoxy-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Fluoro-5-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,5-Dimethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4,5-Dimethyl-2-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Chloro-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Isopropyl-6-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Difluoromethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Isopropyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Ethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Butoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   4-{3-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzoic     acid ethyl ester; -   1-(4-Butyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,6-Dibromo-4-isopropyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(4-trifluoromethylsulfanyl-phenyl)-urea; -   5-{3-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-isophthalic     acid dimethyl ester; -   1-(3-Cyclopentyloxy-4-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   3-{3-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzoic     acid ethyl ester; -   1-(5-tert-Butyl-2-hydroxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Hydroxymethyl-4-phenyl-cyclohexyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methylsulfanyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(4-pentyloxy-biphenyl-3-yl)-urea; -   4-Methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzoic     acid methyl ester; -   1-(2,5-Diethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-Benzothiazol-6-yl-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(2,5-Diethoxy-4-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-benzamide; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-phenoxy-phenyl)-urea; -   1-(5-Ethanesulfonyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   4-Methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-N-phenyl-benzamide; -   1-(2-Methyl-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,3-Dimethyl-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-Butyl-4-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzenesulfonamide; -   1-[3-(2-Methyl-[1,3]dioxolan-2-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Methoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,4-Dimethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methyl-4-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methoxy-4-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Chloro-2-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Chloro-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3,5-Dimethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(4-trifluoromethoxy-phenyl)-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethylsulfanyl-phenyl)-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(2-phenoxy-phenyl)-urea; -   1-(2-Methoxy-5-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Chloro-2,4-dimethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3,5-Bis-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-tert-Butyl-5-methyl-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Methyl-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-tert-Butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methyl-biphenyl-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-tert-Butyl-biphenyl-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Chloro-2,4-dimethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Isopropyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-sec-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-3-propyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxymethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-(4-{6-[(3-methoxy-propyl)-methyl-amino]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-imidazol-1-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-{4-[6-(3-methoxy-propylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methyl-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-morpholin-4-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-2-chloro-3-methyl-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethyl-phenyl)-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(4-trifluoromethoxy-phenyl)-urea; -   1-[5-(1,1-Dimethyl-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(2-methyl-pyrimidin-5-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-hydroxy-propyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-morpholin-4-yl-3-oxo-propyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(morpholine-4-carbonyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; -   2-(5-tert-Butyl-2-methoxy-phenyl)-N-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-acetamide; -   1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-methyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-4-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   2,2,2-Trifluoro-ethanesulfonic acid     (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide     and the pharmaceutically acceptable derivatives thereof.

In addtion to the abovementioned representative compounds the following prophetic compounds of the formula (II) may be useful in the novel methods described herein:

-   1-[4-(6-{[Bis-(2-cyano-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[4-(2-methyl-3-oxo-piperazin-1-ylmethyl)-phenyl]-naphthalen-1-yl}-urea -   1-[4-(6-{[Bis-(2-methoxy-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methyl-3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-114-thiomorpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-{4-[6-(1-oxo-114-thiomorpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-{4-[6-(2-methyl-3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[4-(1-oxo-11-thiomorpholin-4-ylmethyl)-phenyl]-naphthalen-1-yl}-urea; -   1-[4-(4-{[Bis-(2-cyano-ethyl)-amino]-methyl}-phenyl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; -   1-(2-Methoxy-5-pentafluoroethyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; -   1-(2-Methoxy-5-trifluoromethyl-pyridin-3-yl)-3-{4-[2-(4-oxo-piperidin-1-ylmethyl)-pyrimidin-5-yl]-naphthalen-1-yl}-urea; -   1-(2-Methoxy-5-trimethylsilanyl-phenyl)-3-{4-[4-(tetrahydro-pyran-4-ylamino)-phenyl]-naphthalen-1-yl}-urea; -   1-(3-Methoxy-naphthalen-2-yl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; -   1-(3-Methyl-naphthalen-2-yl)-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(3-tert-Butyl-5-methanesulfinyl-phenyl)-3-{4-[6-(1-methyl-piperidin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(3-tert-Butyl-phenyl)-3-[4-(3-pyridin-3-yl-propoxy)-naphthalen-1-yl]-urea; -   1-(3-tert-Butyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(4-Methoxy-biphenyl-3-yl)-3-{4-[4-(tetrahydro-pyran-4-ylmethyl)-imidazol-1-yl]-naphthalen-1-yl}-urea; -   1-(4-Methyl-biphenyl-3-yl)-3-{4-[4-(2-pyridin-4-yl-ethyl)-piperazin-1-yl]-naphthalen-1-yl}-urea; -   1-(4-tert-Butyl-biphenyl-2-yl)-3-[4-     pyridin-4-ylmethoxy)-naphthalen-1-yl]-urea; -   1-(4-tert-Butyl-biphenyl-2-yl)-3-{4-[2-(1-oxo-114-thiomorpholin-4-ylmethyl)-3H-imidazol-4-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-hydroxy-phenyl)-3-[4-(5-morpholin-4-ylmethyl-pyrazin-2-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-3-propyl-phenyl)-3-{4-[4-(pyrrolidine-1-carbonyl)-phenyl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(4-thiomorpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[4-(tetrahydro-pyran-4-ylamino)-phenyl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-methyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-pyridin-3-yl)-3-{4-[6-(4-oxo-piperidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methyl-benzooxazol-7-yl)-3-[4-(6-pyridin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-phenoxy-phenyl)-3-{4-[6-(tetrahydro-pyran-4-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-pyrrolidin-1-yl-phenyl)-3-[4-(4-methoxy-6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-pyrrolidin-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-3-cyano-2-methoxy-phenyl)-3-{4-[2-(2,6-dimethyl-morpholin-4-ylmethyl)-pyrimidin-5-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-4′-dimethylamino-biphenyl-3-yl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-(6-Methoxy-3,3-dimethyl-indan-5-yl)-3-{4-[4-(morpholine-4-carbonyl)-phenyl]-naphthalen-1-yl}-urea; -   1-(6-tert-Butyl-2-chloro-3-methyl-pyridin-4-yl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-benzo[1,3]dioxol-4-yl)-3-{4-[6-(morpholin-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(7-Methoxy-1,4,4-trimethyl-1,2,3,4-tetrahydro-quinolin-6-yl)-3-{4-[6-(tetrahydro-pyran-4-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(7-tert-Butyl-2,4-dimethyl-benzooxazol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[2-Methoxy-5-(1-methyl-1-phenyl-ethyl)-phenyl]-3-{4-[6-(2-pyridin-4-yl-ethyl)-pyridazin-3-yl]-naphthalen-1-yl}-urea; -   1-[2-Methoxy-5-(1-methyl-cyclohexyl)-phenyl]-3-{4-[4-(1-methyl-piperidin-4-ylsulfanyl)-phenyl]-naphthalen-1-yl}-urea; -   1-[2-Methoxy-5-(1-methyl-cyclopropyl)-phenyl]-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-[2-Methoxy-5-(2-methyl-tetrahydro-furan-2-yl)-phenyl]-3-[4-(5-morpholin-4-ylmethyl-pyridin-2-yl)-naphthalen-1-yl]-urea; -   1-[2-Methoxy-5-(3-trifluoromethyl-bicyclo[1.1.1]pent-1-yl)-phenyl]-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-[3-tert-Butyl-5-(1-methyl-1H-imidazol-4-yl)-phenyl]-3-[4-(5-morpholin-4-ylmethyl-pyridin-2-yl)-naphthalen-1-yl]-urea; -   1-[3-tert-Butyl-5-(2-pyrrolidin-1-yl-ethyl)-phenyl]-3-{4-[6-(1-methyl-piperidin-4-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-[3-tert-Butyl-5-(3-pyrrolidin-1-yl-prop-1-ynyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Imidazol-1-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-[2-methoxy-5-(1-phenyl-cyclopropyl)-phenyl]-urea; -   1-[5-(1,1-Dimethyl-propyl)-2-methoxy-phenyl]-3-[4-(4-thiomorpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-[5-(1-Cyano-cyclopropyl)-2-methoxy-phenyl]-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-[5-(1-Hydroxymethyl-cyclopropyl)-2-methoxy-phenyl]-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-1-(2-diethylamino-ethyl)-2-oxo-1,2-dihydro-pyridin-3-yl]-3-{4-[6-(1-methyl-piperidin-4-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-2-(1H-pyrazol-4-yl)-phenyl]-3-[4-(2-morpholin-4-yl-ethoxy)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(1H-pyrazol-4-yl)-phenyl]-3-{4-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-2-(2,5-dioxo-pyrrolidin-1-yl)-phenyl]-3-{4-[6-(1H-imidazol-2-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-2-(2-methyl-pyrimidin-5-yl)-phenyl]-3-[4-(5-pyridin-4-ylmethyl-pyridin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(2-morpholin-4-yl-2-oxo-ethoxy)-phenyl]-3-{4-[6-(2-pyridin-4-yl-ethyl)-pyridazin-3-yl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-2-(2-morpholin-4-yl-2-oxo-ethylamino)-phenyl]-3-{4-[4-(1-methyl-     piperidin-4-ylamino)-piperidin-1-yl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-2-(6-methyl-pyridin-3-yl)-phenyl]-3-{4-[5-(2-pyrrolidin-1-yl-ethyl)-pyridin-2-yl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-2-methoxy-3-(3-morpholin-4-yl-3-oxo-propenyl)-phenyl]-3-[4-(6-pyrrolidin-1-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2-diethylamino-ethoxy)-2-methoxy-phenyl]-3-{4-[4-(tetrahydro-pyran-4-yloxy)-phenyl]-naphthalen-1-yl}-urea; -   1-[5-tert-Butyl-3-(2-pyrrolidin-1-yl-ethyl)-benzofuran-7-yl]-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-[6-tert-Butyl-4-(2-dimethylamino-ethyl)-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-3-{4-[6-(thiomorpholin-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-{5-tert-Butyl-2-methoxy-3-[2-(1-methyl-piperidin-4-yloxy)-ethyl]-phenyl}-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   2-(4-tert-Butyl-2-{3-[4-(5-pyrrolidin-1-ylmethyl-pyridin-2-yl)-naphthalen-1-yl]-ureido}-phenoxy)-N-methyl-acetamide; -   2-[4-tert-Butyl-2-(3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-ureido)-phenoxy]-acetamide; -   3-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-pyrrolidin-1-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acrylamide; -   3-{3-tert-Butyl-5-[3-(4-{4-[2-(1-oxo-114-thiazolidin-3-yl)-ethyl]-phenyl}-     naphthalen-1-yl)-ureido]-phenyl}-N,N-dimethyl-propionamide; -   3-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-benzamide; -   4-tert-Butyl-2-{3-[4-(2-chloro-4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-ureido}-benzamide; -   N-(4-tert-Butyl-2-{3-[4-(6-oxo-1,6-dihydro-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-2-morpholin-4-yl-acetamide; -   N-[3-tert-Butyl-5-(3-{4-[5-(tetrahydro-pyran-4-ylamino)-pyridin-2-yl]-naphthalen-1-yl}-ureido)-phenyl]-2-morpholin-4-yl-acetamide; -   N-[4-tert-Butyl-2-(3-{4-[4-(1-methyl-piperidin-4-yloxy)-phenyl]-naphthalen-1-yl}-ureido)-phenyl]-acetamide     and the pharmaceutically acceptable derivatives thereof.

In another embodiment of the invention there are provided the following compounds of formula (II) which are useful in the novel methods described herein:

-   1-(2-tert-Butyl-5-methyl-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Methyl-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-tert-Butyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(3-tert-Butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methyl-biphenyl-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-tert-Butyl-biphenyl-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Chloro-2,4-dimethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Isopropyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-sec-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-3-propyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxymethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(4-thiomorpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[4-(tetrahydro-pyran-4-ylamino)-phenyl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-methyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-(4-{6-[(3-methoxy-propyl)-methyl-amino]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-imidazol-1-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-{4-[6-(3-methoxy-propylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methyl-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-morpholin-4-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-2-chloro-3-methyl-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-2-chloro-3-methyl-pyridin-4-yl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[2-Methoxy-5-(1-methyl-cyclopropyl)-phenyl]-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethyl-phenyl)-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(4-trifluoromethoxy-phenyl)-urea; -   1-[5-(1,1-Dimethyl-propyl)-2-methoxy-phenyl]-3-[4-(4-thiomorpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-urea; -   1-[5-(1,1-Dimethyl-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(1-Cyano-cyclopropyl)-2-methoxy-phenyl]-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(2-methyl-pyrimidin-5-yl)-phenyl]-3-[4-(5-pyridin-4-ylmethyl-pyridin-2-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(2-methyl-pyrimidin-5-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-hydroxy-propyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-morpholin-4-yl-3-oxo-propyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(morpholine-4-carbonyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   2-[4-tert-Butyl-2-(3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-ureido)-phenoxy]-acetamide; -   3-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-benzamide; -   4-tert-Butyl-2-{3-[4-(2-chloro-4-morpholin-4-ylmethyl-phenyl)-naphthalen-1-yl]-ureido}-benzamide;     and the pharmaceutically acceptable derivatives thereof.

In another embodiment of the invention there are provided the following compounds of formula (II) which are useful in the novel methods described herein:

-   1-(2-tert-Butyl-5-methyl-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-tert-Butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Methyl-biphenyl-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-tert-Butyl-biphenyl-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Isopropyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-sec-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxymethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-(4-{6-[(3-methoxy-propyl)-methyl-amino]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(1,1-Dimethyl-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(2-methyl-pyrimidin-5-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-hydroxy-propyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(morpholine-4-carbonyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide     and the pharmaceutically acceptable derivatives thereof.

In a fourth broad generic aspect, there is provided a method of treating a cytokine mediated disease or condition chosen from: acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the formula (III) disclosed in WO 00/55139 which is the PCT case of U.S. application Ser. No. 09/505,582:

-   -   wherein:     -   E is carbon or a heteroatom group chosen from —O—, —NH— and —S—;     -   G is:         an aromatic C₆₋₁₀ carbocycle or a nonaromatic C₃₋₁₀carbocycle         saturated or unsaturated;         a 6-14 membered monocyclic, bicyclic or tricyclic heteroaryl         containing 1 or more heteroatoms chosen from O, N and S;         a 6-8 membered monocyclic heterocycle containing one or more         heteroatoms chosen from O, N and S; or         an 8-11 membered bicyclic heterocycle, containing one or more         heteroatoms chosen from O, N and S;         wherein G is optionally substituted by one or more R₁, R₂ or R₃;     -   Ar is:         phenyl, naphthyl, quinolinyl, isoquinolinyl, tetrahydronaphthyl,         tetrahydroquinolinyl, tetrahydroisoquinolinyl, benzimidazolyl,         benzofuranyl, dihydrobenzofuranyl, indolinyl, benzothienyl,         dihydrobenzothienyl, indanyl, indenyl or indolyl each being         optionally substituted by one or more R₄ or R₅;     -   X is:         a C₅₋₈ cycloalkyl or cycloalkenyl optionally substituted with         one to two oxo groups or one to three C₁₋₄ alkyl, C₁₋₄ alkoxy or         C₁₋₄ alkylamino chains each being branched or unbranched;         aryl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl,         pyridinyl, pyrimidinyl, pyridinonyl, dihydropyridinonyl,         maleimidyl, dihydromaleimidyl, piperdinyl, benzimidazole,         3H-imidazo[4,5-b]pyridine, piperazinyl, pyridazinyl or         pyrazinyl; each being optionally independently substituted with         one to three C₁₋₄ alkyl, C₁₋₄alkoxy, hydroxy, nitrile, amino,         mono- or di-(C₁₋₃ alkyl)amino, mono- or di-(C₁₋₃         alkylamino)carbonyl, NH₂C(O), C₁₋₆ alkyl-S(O)_(m) or halogen;     -   Y is:         a bond or a C₁₋₄ saturated or unsaturated branched or unbranched         carbon chain optionally partially or fully halogenated, wherein         one or more C atoms are optionally replaced by O, N, or S(O)_(m)         and wherein Y is optionally independently substituted with one         to two oxo groups, nitrile, phenyl or one or more C₁₋₄ alkyl         optionally substituted by one or more halogen atoms;     -   Z is:         aryl, heteroaryl selected from pyridinyl, piperazinyl,         pyrimidinyl, pyridazinyl, pyrazinyl, imidazolyl, pyrazolyl,         triazolyl, tetrazolyl, furanyl, thienyl and pyranyl, heterocycle         selected from tetrahydropyrimidonyl, cyclohexanonyl,         cyclohexanolyl, 2-oxa- or 2-thia-5-aza-bicyclo[2.2.1]heptanyl,         pentamethylene sulfidyl, pentamethylene sulfoxidyl,         pentamethylene sulfonyl, tetramethylene sulfidyl, tetramethylene         sulfoxidyl or tetramethylene sulfonyl, tetrahydropyranyl,         tetrahydrofuranyl, 1,3-dioxolanonyl, 1,3-dioxanonyl,         1,4-dioxanyl, morpholino, thiomorpholino, thiomorpholino         sulfoxidyl, thiomorpholino sulfonyl, piperidinyl, piperidinonyl,         pyrrolidinyl and dioxolanyl, each of the aforementioned Z are         optionally substituted with one to three halogen, C₁₋₆ alkyl,         C₁₋₆ alkoxy, C₁₋₃ alkoxy-C₁₋₃ alkyl, C₁₋₆ alkoxycarbonyl, aroyl,         C₁₋₃acyl, oxo, hydroxy, pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃         alkyl, tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl,         nitrile, carboxy, phenyl wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or         mono- or di-(C₁₋₃ alkyl)amino, C₁₋₆ alkyl-S(O)_(m), or         phenyl-S(O)_(m) wherein the phenyl ring is optionally         substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy,         halogen or mono- or di-(C₁₋₃ alkyl)amino;         or Z is optionally substituted with one to three amino or         amino-C₁₋₃ alkyl wherein the N atom is optionally independently         mono- or di-substituted by aminoC₁₋₆alkyl, C₁₋₃alkyl,         arylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl, C₁₋₅ alkoxy, aroyl,         C₁₋₃acyl, C₁₋₃alkyl-S(O)_(m)— or arylC₀₋₃alkyl-S(O)_(m)— each of         the aforementioned alkyl and aryl attached to the amino group is         optionally substituted with one to two halogen, C₁₋₆ alkyl or         C₁₋₆ alkoxy;         or Z is optionally substituted with one to three aryl,         heterocycle or heteroaryl as hereinabove described in this         paragraph each in turn is optionally substituted by halogen,         C₁₋₆ alkyl or C₁₋₆ alkoxy;         or Z is hydroxy, halogen, nitrile, amino wherein the N atom is         optionally independently mono- or di-substituted by C₁₋₃acyl,         C₁₋₆alkyl or C₁₋₃alkoxyC₁₋₃alkyl, C₁₋₆alkyl branched or         unbranched, C₁₋₆alkoxy, C₁₋₃acylamino, nitrileC₁₋₄alkyl, C 1₆         alkyl-S(O)_(m), and phenyl-S(O)_(m), wherein the phenyl ring is         optionally substituted with one to two halogen, C₁₋₆ alkoxy,         hydroxy or mono- or di-(C₁₋₃ alkyl)amino;     -   each R₁ is independently:         C₁₋₁₀ alkyl branched or unbranched optionally partially or fully         halogenated, wherein one or more C atoms are optionally         independently replaced by O, N or S(O)_(m), and wherein said         C₁₋₁₀ alkyl is optionally substituted with one to three C₃₋₁₀         cycloalkyl, hydroxy, oxo, phenyl, naphthyl, pyridinyl,         pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, pyrrolidinyl,         imidazolyl, pyrazolyl, thienyl, furyl, dioxolanyl, isoxazolyl or         isothiazolyl; each of the aforementioned being optionally         substituted with one to five groups selected from halogen, C₁₋₆         alkyl which is optionally partially or fully halogenated, C₃₋₈         cycloalkanyl, C₅₋₈ cycloalkenyl, hydroxy, nitrile, C₁₋₃ alkoxy         which is optionally partially or fully halogenated or NH₂C(O),         mono- or di(C₁₋₃ alkyl)amino, and mono- or         di(C₁₋₃alkyl)aminocarbonyl;         or R₁ is         cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, or         cycloheptyloxy each being optionally partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups optionally partially or fully halogenated, nitrile,         hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloalkyl group         wherein one to three ring methylene groups are independently         replaced by O, S(O)_(m), CHOH, >C═O, >C═S or NH;         phenyloxy or benzyloxy each being optionally partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups optionally partially or fully halogenated, nitrile,         hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloaryl group         wherein one to two ring methyne groups are independently         replaced by N;         cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl,         bicyclopentanyl, bicyclohexanyl or bicycloheptanyl, each being         optionally partially or fully halogenated and optionally         substituted with one to three C₁₋₃ alkyl optionally partially or         fully halogenated, nitrile, hydroxyC₁₋₃alkyl or aryl; or an         analog of such cycloalkyl group wherein one to three ring         methylene groups are independently replaced by O, S(O)_(m),         CHOH, >C═O, >C═S or NH;         C₃₋₁₀ branched or unbranced alkenyl each being optionally         partially or fully halogenated, and optionally substituted with         one to three C₁₋₅ branched or unbranched alkyl, phenyl,         naphthyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl,         pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl or         isothiazolyl, each of the aforementioned being substituted with         one to five halogen, C₁₋₆ alkyl which is optionally partially or         fully halogenated, cyclopropanyl, cyclobutanyl, cyclopentanyl,         cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl and         bicycloheptanyl, hydroxy, nitrile, C₁₋₃ alkyloxy which is         optionally partially or fully halogenated, NH₂C(O), mono- or         di(C₁₋₃alkyl)aminocarbonyl; the C₃₋₁₀ branched or unbranced         alkenyl being optionally interrupted by one or more heteroatoms         chosen from O, N and S(O)_(m);         cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,         cycloheptadienyl, bicyclohexenyl or bicycloheptenyl, wherein         such cycloalkenyl group is optionally substituted with one to         three C₁₋₃ alkyl groups;         oxo, nitrile, halogen;         silyl containing three C₁₋₄ alkyl groups optionally partially or         fully halogenated; or         C₃₋₆ alkynyl branched or unbranched carbon chain optionally         partially or fully halogenated, wherein one or more methylene         groups are optionally replaced by O, NH or S(O)_(m) and wherein         said alkynyl group is optionally independently substituted with         one to two oxo groups, hydroxy, pyrroldinyl, pyrrolyl,         tetrahydropyranyl, one or more C₁₋₄ alkyl optionally substituted         by one or more halogen atoms, nitrile, morpholino, piperidinyl,         piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono-         or di(C₁₋₃ alkyl)amino optionally substituted by one or more         halogen atoms;     -   each R₂, R₄, and R₅ is         a C₁₋₆ branched or unbranched alkyl optionally partially or         fully halogenated, C₁₋₆acyl, aroyl, C₁₋₄ branched or unbranched         alkoxy, each being optionally partially or fully halogenated,         halogen, methoxycarbonyl, C₁₋₃ alkyl-S(O)_(m) optionally         partially or fully halogenated, or phenyl-S(O)_(m);         OR₆, C₁₋₆ alkoxy, hydroxy, nitrile, nitro, halogen;         or amino-S(O)_(m)— wherein the N atom is optionally         independently mono- or di-substituted by C₁₋₆alkyl or         arylC₀₋₃alkyl, or amino wherein the N atom is optionally         independently mono- or di-substituted by C₁₋₃alkyl,         arylC₀₋₃alkyl, C₁₋₆acyl, C₁₋₆alkyl-S(O)_(m)— or         arylC₀₋₃alkyl-S(O)_(m)—, each of the aforementioned alkyl and         aryl in this subparagraph are optionally partially or fully         halogenated and optionally substituted with one to two C₁₋₆         alkyl or C₁₋₆ alkoxy;     -   each R₃ is independently:         phenyl, naphthyl, morpholino, pyridinyl, pyrimidinyl, pyrazinyl,         pyridazinyl, pyrrolyl, pyrrolidinyl, imidazolyl, pyrazolyl,         thiazolyl, oxazoyl, [1,3,4]oxadiazol, triazolyl, tetrazolyl,         thienyl, furyl, tetrahydrofuryl, isoxazolyl, isothiazolyl,         quinolinyl, isoquinolinyl, indolyl, benzimidazolyl,         benzofuranyl, benzoxazolyl, benzisoxazolyl, benzpyrazolyl,         benzothiofuranyl, cinnolinyl, pterindinyl, phthalazinyl,         naphthypyridinyl, quinoxalinyl, quinazolinyl, purinyl or         indazolyl, each of the aforementioned is optionally substituted         with one to three phenyl, naphthyl, heterocycle or heteroaryl as         hereinabove described in this paragraph, C₁₋₆ branched or         unbranched alkyl which is optionally partially or fully         halogenated, cyclopropanyl, cyclobutanyl, cyclopentanyl,         cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl,         bicycloheptanyl, phenyl C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl,         halogen, hydroxy, oxo, nitrile, C₁₋₃ alkoxy optionally partially         or fully halogenated, phenyloxy, naphthyloxy, heteroaryloxy or         heterocyclicoxy wherein the heterocyclic or heteroaryl moiety is         as hereinabove described in this paragraph, nitro, amino, mono-         or di-(C₁₋₃alky)lamino, phenylamino, naphthylamino, heteroaryl         or heterocyclic amino wherein the heteroaryl heterocyclic moiety         is as hereinabove described in this paragraph, NH₂C(O), a mono-         or di-(C₁₋₃alkyl) aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl,         amino-C₁₋₅ alkyl, mono- or di-(C₁₋₅alkyl)amino, mono- or         di-(C₁₋₃alkyl)amino-C₁₋₅ alkyl, amino-S(O)₂,         di-(C₁₋₃alkyl)amino-S(O)₂, R₇—C₁₋₅ alkyl, R₈—C₁₋₅ alkoxy,         R₉—C(O)—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkyl(R₁₁)N, carboxy-mono- or         di-(C₁₋₅alkyl)-amino;         a fused aryl selected from benzocyclobutanyl, indanyl, indenyl,         dihydronaphthyl, tetrahydronaphthyl, benzocycloheptanyl and         benzocycloheptenyl, or a fused heteroaryl selected from         cyclopentenopyridinyl, cyclohexanopyridinyl,         cyclopentanopyrimidinyl, cyclohexanopyrimidinyl,         cyclopentanopyrazinyl, cyclohexanopyrazinyl,         cyclopentanopyridazinyl, cyclohexanopyridazinyl,         cyclopentanoquinolinyl, cyclohexanoquinolinyl,         cyclopentanoisoquinolinyl, cyclohexanoisoquinolinyl,         cyclopentanoindolyl, cyclohexanoindolyl,         cyclopentanobenzimidazolyl, cyclohexanobenzimidazolyl,         cyclopentanobenzoxazolyl, cyclohexanobenzoxazolyl,         cyclopentanoimidazolyl, cyclohexanoimidazolyl,         cyclopentanothienyl and cyclohexanothienyl; wherein the fused         aryl or fused heteroaryl ring is independently substituted with         zero to three phenyl, naphthyl, pyridinyl, pyrimidinyl,         pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl,         thienyl, furyl, isoxazolyl, isothiazolyl, C₁₋₆ alkyl which is         optionally partially or fully halogenated, halogen, nitrile,         C₁₋₃ alkyloxy which is optionally partially or fully         halogenated, phenyloxy, naphthyloxy, heteroaryloxy or         heterocyclicoxy wherein the heteroaryl or heterocyclic moiety is         as hereinabove described in this paragraph, nitro, amino, mono-         or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl         or heterocyclic amino wherein the heteroaryl or heterocyclic         moiety is as hereinabove described in this paragraph, NH₂C(O),         mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₄ alkyl-OC(O), C₁₋₅         alkyl-C(O)—C₁₋₄ alkyl, amino-C₁₋₅ alkyl, mono- or         di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, R₁₂—C₁₋₅ alkyl, R₁₃—C₁₋₅ alkoxy,         R₁₄—C(O)—C₁₋₅ alkyl or R₁₅—C₁₋₅ alkyl(R₁₆)N;         cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl,         cycloheptanyl, bicyclopentanyl, bicyclohexanyl or         bicycloheptanyl, each being optionally be partially or fully         halogenated and optionally substituted with one to three C₁₋₃         alkyl groups, or an analog of such cycloalkyl group wherein one         to three ring methylene groups are independently replaced by O,         S, CHOH, >C═O, >C═S or NH;         cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,         cycloheptadienyl, bicyclohexenyl or bicycloheptenyl, each         optionally substituted with one to three C₁₋₃ alkyl groups;         C₁₋₄ alkyl-phenyl-C(O)—C₁₋₄ alkyl-, C₁₋₄ alkyl-C(O)—C₁₋₄ alkyl-         or C₁₋₄ alkyl-phenyl-S(O)_(m)—C₁₋₄ alkyl-;         C₁₋₆ alkyl or C₁₋₆ branched or unbranched alkoxy each of which         is optionally partially or fully halogenated or optionally         substituted with R₁₇;         OR₁₈ or C₁₋₆ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₅alkyl)amino optionally substituted         with R₁₉;         R₂₀C(O)N(R₂₁)—, R₂₂O— or R₂₃R₂₄NC(O)—; R₂₆(CH₂)_(m)C(O)N(R₂₁)—,         R₂₃R₂₄NC(O)—C₁₋₃alkoxy or R₂₆C(O)(CH₂)_(m)N(R₂₁)—;         C₂₋₆alkenyl substituted by R₂₃R₂₄NC(O)—;         C₂₋₆ alkynyl branched or unbranched carbon chain, optionally         partially or fully halogenated, wherein one or more methylene         groups are optionally replaced by O, NH, S(O)_(m) and wherein         said alkynyl group is optionally independently substituted with         one to two oxo groups, pyrroldinyl, pyrrolyl, morpholino,         piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl,         tetrazolyl one or more C₁₋₄ alkyl optionally substituted by one         or more halogen atoms, nitrile, morpholino, piperidinyl,         piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono-         or di(C₁₋₄ alkyl)amino optionally substituted by one or more         halogen atoms;         C₁₋₆acyl or aroyl;     -   R₆ is a:         C₁₋₄ alkyl optionally partially or fully halogenated and         optionally substituted with R₂₆;     -   each R₇, R₈, R₉, R₁₀, R₁₂, R₁₃, R₁₄, R₁₅, R₁₇, R₁₉, R₂₅ and R₂₆         is independently: nitrile, phenyl, morpholino, piperidinyl,         piperazinyl, imidazolyl, pyridinyl, tetrazolyl, amino or mono-         or di-(C₁₋₄alkyl)amino optionally partially or fully         halogenated;     -   each R₁₁ and R₁₆ is independently:         hydrogen or C₁₋₄ alkyl optionally partially or fully         halogenated;     -   R₁₈ is independently:         hydrogen or a C₁₋₄ alkyl optionally independently substituted         with oxo or R₂₅;     -   R₂₀ is independently:         C₁₋₁₀ alkyl optionally partially or fully halogenated, phenyl,         or pyridinyl;     -   R₂₁ is independently:         hydrogen or C₁₋₃ alkyl optionally partially or fully         halogenated;     -   each R₂₂, R₂₃ and R₂₄ is independently:         hydrogen, C₁₋₆ alkyl optionally partially or fully halogenated,         said C₁₋₆ alkyl is optionally interrupted by one or more O, N or         S, said C₁₋₆ alkyl also being independently optionally         substituted by mono- or di-(C₁₋₃alkyl)aminocarbonyl, phenyl,         pyridinyl, amino or mono- or di-(C₁₋₄alkyl)amino each of which         is optionally partially or fully halogenated and optionally         substituted with mono- or di-(C₁₋₃alkyl)amino;         or R₂₃ and R₂₄ taken together optionally form a heterocyclic or         heteroaryl ring;

-   m=0, 1 or 2;

-   W is 0 or S and     the pharmaceutically acceptable derivatives thereof.

A preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III) as provided above and wherein:

-   E is —CH₂—, —NH— or —O—; -   W is O;     and -   G is:     phenyl, naphthyl, benzocyclobutanyl, dihydronaphthyl,     tetrahydronaphthyl, benzocycloheptanyl, benzocycloheptenyl, indanyl,     indenyl;     pyridinyl, pyridonyl, quinolinyl, dihydroquinolinyl,     tetrahydroquinoyl, isoquinolinyl, tetrahydroisoquinoyl, pyridazinyl,     pyrimidinyl, pyrazinyl, benzimidazolyl, benzthiazolyl,     benzooxazolyl, benzofuranyl, benzothiophenyl, benzpyrazolyl,     dihydrobenzofuranyl, dibenzofuranyl, dihydrobenzothiophenyl,     benzooxazolonyl, benzo[1,4]oxazin-3-onyl, benzodioxolyl,     benzo[1,3]dioxol-2-onyl, benzofuran-3-onyl, tetrahydrobenzopyranyl,     indolyl, 2,3-dihydro-1H-indolyl, indolinyl, indolonyl, indolinonyl,     phthalimidyl, chromoyl;     oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl,     piperidinyl, piperazinyl, morpholino, tetrahydropyranyl, dioxanyl,     tetramethylene sulfonyl, tetramethylene sulfoxidyl, oxazolinyl,     3,4-dihydro-2H-benzo[1,4]oxazinyl, thiazolinyl, imidazolinyl,     tertrahydropyridinyl, homopiperidinyl, pyrrolinyl,     tetrahydropyrimidinyl, decahydroquinolinyl, decahydroisoquinolinyl,     thiomorpholino, thiazolidinyl, dihydrooxazinyl, dihydropyranyl,     oxocanyl, heptacanyl, thioxanyl or dithianyl; wherein G is     optionally substituted by one or more R₁, R₂ or R₃.

A more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III) as provided above and wherein:

-   -   E is —NH—;     -   G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl,         isoquinolinyl, pyrazinyl, benzimidazolyl, benzooxazolyl,         benzooxazolonyl, benzofuranyl, benzothiophenyl, benzpyrazolyl,         dihydrobenzofuranyl, dihydrobenzothiophenyl,         3,4-dihydro-2H-benzo[1,4]oxazinyl, indanyl, indenyl, indolyl,         indolinyl, indolonyl, 2,3-dihydro-1H-indolyl or indolinonyl,         wherein G is optionally substituted by one or more R₁, R₂ or R₃;     -   Ar is:         naphthyl, quinolinyl, isoquinolinyl, tetrahydronaphthyl,         tetrahydroquinolinyl, tetrahydroisoquinolinyl, indanyl, indenyl         or indolyl each being optionally substituted by one or more R₄         or R₅ groups;     -   X is:         phenyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl,         pyridinyl, pyrimidinyl, pyridinonyl, dihydropyridinonyl,         maleimidyl, dihydromaleimidyl, piperdinyl, piperazinyl,         pyridazinyl or pyrazinyl; each being optionally independently         substituted with one to three C₁₋₄ alkyl, C₁₋₄alkoxy, hydroxy,         nitrile, amino, mono- or di-(C₁₋₃ alkyl)amino, mono- or di-(C₁₋₃         alkylamino)carbonyl, NH₂C(O), C₁₋₆ alkyl-S(O)_(m) or halogen;     -   Y is:         a bond or         a C₁₋₄ saturated or unsaturated carbon chain wherein one or more         of the C atoms is optionally replaced by O, N, or S(O)_(m) and         wherein Y is optionally independently substituted with one to         two oxo groups, nitrile, phenyl or one or more C₁₋₄ alkyl         optionally substituted by one or more halogen atoms;     -   Z is:         phenyl, heteroaryl selected from pyridinyl, piperazinyl,         pyrimidinyl, pyridazinyl, pyrazinyl, imidazolyl, furanyl,         thienyl and pyranyl, heterocycle selected from         2-oxa-5-aza-bicyclo[2.2.1]heptanyl, tetrahydropyrimidonyl,         pentamethylene sulfidyl, pentamethylene sulfoxidyl,         pentamethylene sulfonyl, tetramethylene sulfidyl, tetramethylene         sulfoxidyl tetramethylene sulfonyl, tetrahydropyranyl,         tetrahydrofuranyl, 1,3-dioxolanonyl, 1,3-dioxanonyl,         1,4-dioxanyl, morpholino, thiomorpholino, thiomorpholino         sulfoxidyl, piperidinyl, piperidinonyl, dihydrothiazolyl,         dihydrothiazolyl sulfoxidyl, pyrrolidinyl and dioxolanyl which         are optionally substituted with one to three nitrile, C₁₋₃         alkyl, C₁₋₃ alkoxy, amino, mono- or di-(C₁₋₃ alkyl)amino, CONH₂         or OH;         or Z is optionally substituted by phenyl, heterocycle or         heteroaryl as hereinabove described in this paragraph each in         turn is optionally substituted by halogen, C₁₋₃ alkyl or C₁₋₃         alkoxy;         or Z is nitrile, nitrileC₁₋₃ alkyl, C₁₋₆ alkyl-S(O)_(m),         halogen, hydroxy, C₁₋₃ alkyl, C₁₋₃ acylamino, C₁₋₄ alkoxy,         amino, mono- or di-(C₁₋₃ alkyl)aminocarbonyl, or amino mono or         di-substituted by aminoC₁₋₆ alkyl or C₁₋₃alkoxyC₁₋₃alkyl;     -   each R₁ is independently:         C₁₋₆ alkyl branched or unbranched optionally partially or fully         halogenated, wherein one or more C atoms are optionally         independently replaced by O, N or S(O)_(m), and wherein said         C₁₋₆ alkyl is optionally substituted with one to three         C₃₋₆cycloalkyl, oxo, phenyl, dioxolanyl, pyrrolidinyl, furyl,         isoxazolyl or isothiazolyl; each of the aforementioned being         optionally substituted with one to three groups selected from         halogen, C₁₋₃ alkyl which is optionally partially or fully         halogenated, hydroxy, nitrile and C₁₋₃alkoxy which is optionally         partially or fully halogenated;         cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl,         bicyclopentanyl or bicyclohexanyl, each being optionally         partially or fully halogenated and optionally substituted with         one to three C₁₋₃ alkyl groups optionally partially or fully         halogenated, nitrile, hydroxyC₁₋₃alkyl or phenyl; or an analog         of such cycloalkyl group wherein one to three ring methylene         groups are independently replaced by O, S, CHOH, >C═O, >C═S or         NH;         oxo;         C₃₋₆ alkynyl branched or unbranched carbon chain optionally         partially or fully halogenated, wherein one or more methylene         groups are optionally replaced by O, NH or S(O)_(m) and wherein         said alkynyl group is optionally independently substituted with         one to two oxo groups, hydroxy, pyrroldinyl, pyrrolyl,         tetrahydropyranyl, C₁₋₄ alkyl optionally substituted by one or         more halogen atoms, nitrile, morpholino, piperidinyl,         piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono-         or di(C₁₋₃alkyl)amino optionally substituted by one or more         halogen atoms; or         silyl containing three C₁₋₄ alkyl groups optionally partially or         fully halogenated;     -   R₂ is independently:         a C₁₋₅ branched or unbranched alkyl optionally partially or         fully halogenated, acetyl, aroyl, C₁₋₄ branched or unbranched         alkoxy, each being optionally partially or fully halogenated,         halogen, methoxycarbonyl, C₁₋₂ alkyl-S(O)_(m) optionally         partially or fully halogenated, or phenyl-S(O)_(m);         C₁₋₃ alkoxy, hydroxy, nitrile, nitro, halogen;         or amino-S(O)_(m)— wherein the N atom is optionally         independently mono- or di-substituted by C₁₋₃alkyl or         arylC₀₋₃alkyl, or amino wherein the N atom is optionally         independently mono- or di-substituted by C₁₋₃alkyl,         arylC₀₋₃alkyl, C₁₋₃acyl, C₁₋₄alkyl-S(O)_(m)— or         arylC₀₋₃alkyl-S(O)_(m)—, each of the aforementioned alkyl and         aryl in this subparagraph are optionally partially or fully         halogenated and optionally substituted with one to two C₁₋₃         alkyl or C₁₋₃ alkoxy;     -   R₃ is independently:         phenyl, morpholino, pyridinyl, pyrimidinyl, pyrazinyl, pyrrolyl,         pyrrolidinyl, imidazolyl, [1,3,4]oxadiazol, pyrazolyl, each is         optionally substituted with one to three phenyl, naphthyl,         heterocycle or heteroaryl as hereinabove described in this         paragraph, C₁₋₆ alkyl which is optionally partially or fully         halogenated, cyclopropanyl, cyclobutanyl, cyclopentanyl,         cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl,         bicycloheptanyl, phenyl C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl,         halogen, oxo, hydroxy, nitrile, C₁₋₃ alkoxy optionally partially         or fully halogenated, phenyloxy, naphthyloxy, heteroaryloxy or         heterocyclicoxy wherein the heteroaryl or heterocyclic moiety is         as hereinabove described in this paragraph, nitro, amino, mono-         or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl         or heterocyclic amino wherein the heteroaryl or heterocyclic         moiety is as hereinabove described in this paragraph, NH₂C(O), a         mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄         alkyl, mono- or di-(C₁₋₃alkyl)amino, mono- or         di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, mono- or         di-(C₁₋₃alkyl)amino-S(O)₂, R₇—C₁₋₅ alkyl, R₈—C₁₋₅ alkoxy,         R₉—C(O)—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkyl(R₁₁)N, carboxy-mono- or         di-(C₁₋₅)-alkyl-amino;         C₁₋₃ alkyl or C₁₋₄ alkoxy each being optionally partially or         fully halogenated or optionally substituted with R₁₇;         OR₁₈ or C₁₋₆ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₅ alkyl)amino optionally substituted         with R₁₉;         R₂₀C(O)N(R₂₁)—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)—,         R₂₃R₂₄NC(O)—C₁₋₂alkoxy or R₂₆C(O)CH₂N(R₂₁)—;         C₂₋₄alkenyl substituted by R₂₃R₂₄NC(O)—; or         C₂₋₄ alkynyl branched or unbranched carbon chain optionally         partially or fully halogenated wherein one of the methylene         groups is optionally replaced by O, and optionally independently         substituted with one to two oxo groups, pyrroldinyl, pyrrolyl,         morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl,         pyridinyl, tetrazolyl or one or more C₁₋₄ alkyl optionally         substituted by one or more halogen atoms;         C₁₋₃acyl; and         R₂₃ and R₂₄ taken together optionally form imidazolyl,         piperidinyl, morpholino, piperazinyl or a pyridinyl ring.

A yet more preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III), as described in the immediate previous paragraph, wherein:

G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl, isoquinolinyl, pyrazinyl, 3,4-dihydro-2H-benzo[1,4]oxazinyl, benzothiophenyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, benzooxazolyl, indanyl, indolyl, indolinyl, indolonyl or indolinonyl, wherein G is optionally substituted by one or more R₁, R₂ or R₃;

-   -   Ar is naphthyl;     -   X is         phenyl, imidazolyl, pyridinyl, pyrimidinyl, piperdinyl,         piperazinyl, pyridazinyl or pyrazinyl each being optionally         independently substituted with one to three C₁₋₄ alkyl,         C₁₋₄alkoxy, hydroxy, nitrile, amino, mono- or di-(C₁₋₃         alkyl)amino, mono- or di-(C₁₋₃ alkylamino)carbonyl, NH₂C(O),         C₁₋₆ alkyl-S(O)_(m) or halogen;     -   Y is:         a bond or         a C₁₋₄ saturated carbon chain wherein one or more of the C atoms         is optionally replaced by O, N or S and wherein Y is optionally         independently substituted with nitrile or oxo;     -   Z is:         phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl,         imidazolyl, dihydrothiazolyl, dihydrothiazolyl sulfoxide,         pyranyl, pyrrolidinyl, phenylpiperazinyl, tetrahydropyranyl,         tetrahydrofuranyl, dioxolanyl,         2-oxa-5-aza-bicyclo[2.2.1]heptanyl, morpholino, thiomorpholino,         thiomorpholino sulfoxidyl, piperidinyl, piperidinonyl,         piperazinyl or tetrahydropyrimidonyl each of which are         optionally substituted with one to two C₁₋₂ alkyl or C₁₋₂         alkoxy; or         Z is hydroxy, C₁₋₃ alkyl, C₁₋₃ alkoxy, C₁₋₃ acylamino, C₁₋₃         alkylsulfonyl, nitrile C₁₋₃ alkyl or amino mono or         di-substituted by C₁₋₃ alkoxyC₁₋₃ alkyl;     -   each R₁ is independently:         C₁₋₅ alkyl branched or unbranched optionally partially or fully         halogenated, wherein one or more C atoms are optionally         independently replaced by O, N or S(O)_(m), and wherein said         C₁₋₅ alkyl is optionally substituted with oxo, dioxolanyl,         pyrrolidinyl, furyl or phenyl each optionally substituted with         one to three halogen, C₁₋₃ alkyl which is optionally partially         or fully halogenated, hydroxy, nitrile and C₁₋₃alkoxy which is         optionally partially or fully halogenated;         cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl,         bicyclopentanyl or bicyclohexanyl, each being optionally         partially or fully halogenated and optionally substituted with         one to three C₁₋₃ alkyl groups optionally partially or fully         halogenated, nitrile, hydroxyC₁₋₃alkyl or phenyl; and an analog         of cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl,         bicyclopentanyl or bicyclohexanyl wherein one ring methylene         group is replaced by O;         oxo;         C₂₋₄ alkynyl optionally partially or fully halogenated wherein         one or more methylene groups are optionally replaced by O, and         optionally independently substituted with one to two oxo groups,         hydroxy, pyrroldinyl, pyrrolyl, tetrahydropyranyl, C₁₋₄ alkyl         optionally substituted by one or more halogen atoms, nitrile,         morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl,         pyridinyl, tetrazolyl, or mono- or di(C₁₋₃alkyl)amino optionally         substituted by one or more halogen atoms; or         silyl containing three C₁₋₂ alkyl groups optionally partially or         fully halogenated;     -   each R₂ is independently:         a C₁₋₄ alkyl optionally partially or fully halogenated, C₁₋₄         alkoxy optionally partially or fully halogenated, bromo, chloro,         fluoro, methoxycarbonyl, methyl-S(O)_(m), ethyl-S(O)_(m) each         optionally partially or fully halogenated or phenyl-S(O)_(m);         or R₂ is mono- or di-C₁₋₃acylamino, amino-S(O)_(m) or         S(O)_(m)amino wherein the N atom is mono- or di-substituted by         C₁₋₃alkyl or phenyl, nitrile, nitro or amino;     -   each R₃ is independently:         phenyl, morpholino, pyridinyl, pyrimidinyl, pyrrolidinyl,         2,5-pyrrolidin-dionyl, imidazolyl, [1,3,4]oxadiazol, pyrazolyl,         each of the aforementioned is optionally substituted with one to         three C₁₋₃ alkyl which is optionally partially or fully         halogenated, halogen, oxo, hydroxy, nitrile and C₁₋₃ alkoxy         optionally partially or fully halogenated;         C₁₋₃ alkyl or C₁₋₃ alkoxy optionally partially or fully         halogenated or optionally substituted with R₁ ₇;         OR₁₈ or C₁₋₃ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₃ alkyl)amino optionally substituted         with R₁₉;         R₂₀C(O)N(R₂₁)—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)—,         NH₂C(O)methoxy or R₂₆C(O)CH₂N(R₂₁)—;         C₂₋₄ alkenyl substituted by R₂₃R₂₄NC(O)—; or         C₂₋₄ alkynyl substituted with pyrroldinyl or pyrrolyl;         C₁₋₃acyl and         R₂₃ and R₂₄ taken together optionally form morpholino.

A yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III), as described in the immediate previous paragraph, and wherein:

G is phenyl, pyridinyl, pyridonyl, 2-naphthyl, quinolinyl, isoquinolinyl, dihydrobenzofuranyl, indanyl, 5-indolyl, 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl, benzooxalolyl, 2,3-dihydrobenzooxazol-7-yl, 2-oxo-2,3-dihydro-1H-indol-5-yl, indolinyl, indolonyl, or indolinonyl, wherein G is optionally substituted by one or more R₁, R₂ or R₃;

-   -   Ar is 1-naphthyl;     -   X is:         phenyl, imidazolyl, pyridinyl, pyrimidinyl, piperdinyl,         piperazinyl, pyridazinyl or pyrazinyl;     -   Y is:         a bond or         —CH₂—, —CH₂CH₂—, —C(O)—, —O—, —S—, —NH—CH₂CH₂CH₂—, —N(CH₃)—,         CH₂(CN)CH₂—NH—CH₂ or —NH—;     -   Z is         morpholino, dioxolanyl, tetrahydrofuranyl, pyridinyl,         2-oxa-5-aza-bicyclo[2.2.1]heptanyl, C₁₋₃alkoxyphenylpiperazinyl,         hydroxy, C₁₋₃alkyl, N,N-diC₁₋₃alkoxyC₁₋₃alkylamino,         C₁₋₃acylamino, C₁₋₃alkylsulfonyl or nitrileC₁₋₃alkyl;         each R₁ is independently:         C₁₋₅ alkyl optionally partially or fully halogenated wherein one         or more C atoms are optionally independently replaced by O or N,         and wherein said C₁₋₅ alkyl is optionally substituted with oxo,         dioxolanyl, pyrrolidinyl, furyl or phenyl optionally substituted         by C₁₋₃alkoxy;         cyclopropyl, cyclopentanyl, cyclohexanyl and bicyclopentanyl         optionally substituted with one to three methyl groups         optionally partially or fully halogenated, nitrile,         hydroxymethyl or phenyl; or 2-tetrahydrofuranyl substituted by         methyl; or trimethyl silyl;         propynyl substituted hydroxy or tetrahydropyran-2-yloxy;     -   R₂ is         is mono- or di-C₁₋₃acylamino, amino-S(O)_(m) or S(O)_(m) amino         wherein the N atom is mono- or di-substituted by C₁₋₃alkyl or         phenyl, bromo, chloro, fluoro, nitrile, nitro, amino,         methylsulfonyl optionally partially or fully halogenated or         phenylsulfonyl;     -   each R₃ is independently:         phenyl, morpholino, pyridinyl, pyrimidinyl, pyrrolidinyl,         2,5-pyrrolidin-dionyl, imidazolyl, [1,3,4]oxadiazol or         pyrazolyl, each is optionally substituted with C₁₋₂ alkyl which         is optionally partially or fully halogenated;         C₁₋₃ alkyl or C₁₋₃ alkoxy each being optionally partially or         fully halogenated or optionally substituted with diethylamino;         OR₁₈ or C₁₋₃ alkyl optionally substituted with OR₁₈;         amino or mono- or di-(C₁₋₃ alkyl)amino optionally substituted         with R₁₉;         CH₃C(O)NH—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)—,         NH₂C(O)methoxy or R₂₆C(O)CH₂N(R₂₁)—;         C₂₋₄alkenyl substituted by R₂₃R₂₄NC(O)—; or         C₂₋₄ alkynyl substituted with pyrroldinyl or pyrrolyl;         C₁₋₂acyl; and         R₂₃ and R₂₄ are H or R₂₃ and R₂₄ taken together optionally form         morpholino; and         R₂₆ is morpholino.

A further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III), as described in the immediate previous paragraph, and wherein:

-   -   G is         phenyl, pyridinyl, 5-indolyl,         3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl, benzooxalolyl,         2,3-dihydrobenzooxazol-7-yl, 2-oxo-2,3-dihydro-1H-indol-5-yl or         2-naphthyl wherein G is optionally substituted by one or more         R₁, R₂ or R₃;     -   X is:         imidazolyl, pyridinyl, pyrimidinyl or pyrazinyl;     -   Y is:         a bond, CH₂(CN)CH₂—NH—CH₂, —CH₂—, —NH—CH₂CH₂CH₂— or —NH—;     -   Z is morpholin-4yl, dioxolan-2yl, tetrahydrofuranyl, pyridinyl,         2-oxa-5-aza-bicyclo[2.2.1]hept-5yl, methoxyphenylpiperazinyl,         hydroxy, methyl, N,N-dimethoxyethylamino, acetylamino,         methylsulfonyl or cyanoethyl;     -   each R₁ is independently:         tert-butyl, sec-butyl, tert-amyl, phenyl,         tetrahydropyran-2-yloxypropynyl, hydroxypropynyl, trihalomethyl,         2,2-diethylpropionyl or cyclohexanyl;     -   R₂ is chloro, nitro, amino, nitrile, methylsulfonylamino,         diacetylamino, phenylsulfonylamino, N,N-di(methylsulfonyl)amino,         methylsulfonyl or trihalomethylsulfonyl;     -   R₃ is independently:         methyl, C₁₋₃ alkoxy, methoxymethyl, hydroxypropyl,         dimethylamino, C₁₋₄alkylamino, NH₂C(O)methoxy, acetyl,         pyrrolidinyl, imidazolyl, pyrazolyl, morpholino or         morpholinocarbonyl.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III), as described in the immediate previous paragraph, and wherein:

-   -   X is pyridinyl.

A still yet further preferred subgeneric aspect of the invention comprises a method of using the compounds of the formula (III), as described immediately above, and wherein

-   -   the pyridinyl is attached to Ar via the 3-pyridinyl position.

The following compounds are representative of the compounds of formula (II) which are useful in the novel methods described herein:

-   1-(4-tert-Butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; -   1-(6-Chloro-4-trifluoromethyl-pyridin-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(4-Difluoromethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Methyl-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[2-Methoxy-5-(1-methyl-1-phenyl-ethyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   (5-tert-Butyl-2-methyl-phenyl)-carbamic acid     3-(5-{4-[3-(5-tert-butyl-2-methyl-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylamino)-propyl     ester; -   1-(6-tert-Butyl-benzo[1,3]dioxol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; -   1,3-Bis-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,3-Dimethyl-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(2-p-tolyloxy-5-trifluoromethyl-phenyl)-urea; -   1-[2-(2-Methoxy-phenoxy)-5-trifluoromethyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-naphthalen-1-yl-urea; -   1-{5-tert-Butyl-2-methyl-3-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-{5-tert-Butyl-2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Hydroxymethyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methoxy-dibenzofuran-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,5-Di-tert-butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[3-(4-Bromo-1-methyl-1H-pyrazol-3-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Hydroxy-5,6,7,8-tetrahydro-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(1-Acetyl-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-oxazol-5-yl-phenyl)-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-[1,3,4]oxadiazol-2-yl-phenyl)-urea; -   1-(2-Methoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   Furan-2-carboxylic acid     (4-tert-butyl-2-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; -   1-(2-Methoxy-4-phenylamino-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-Methoxy-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Hydroxy-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N,N-Diethyl-4-methoxy-3-{3-[4-(6-     morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzenesulfonamide; -   1-(2,2-Difluoro-benzo[1,3]dioxol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(1,1-Dimethyl-propyl)-2-phenoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(2,2-Dimethyl-propionyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   2-Chloro-5-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzoic     acid isopropyl ester; -   1-(4-Amino-3,5-dibromo-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(3-hydroxy-prop-1-ynyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-hydroxy-prop-1-ynyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butoxy-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(1-Cyano-cyclopropyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2-diethylamino-ethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-[1,3]dioxolan-2-yl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-pyrrolidin-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-dimethylamino-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-propoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-hydroxymethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   2-(5-tert-Butyl-2-methoxy-phenyl)-N-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-acetamide; -   1-(2-Methoxy-5-phenoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-cyclopentyloxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-pyridin-3-yl-pyrrolidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-Cyclohexyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,4-Dimethoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-methyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-Acetyl-N-(5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; -   1-(6-tert-Butyl-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[6-tert-Butyl-4-(2-morpholin-4-yl-ethyl)-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-isopropoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-imidazol-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-4-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide; -   1-(5-tert-Butyl-3-ethylamino-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-bis(methanesulfon)amide; -   1-[5-tert-Butyl-2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methanesulfinyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Ethanesulfonyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-{[Bis-(2-methoxy-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-dimethylamino-pyrrolidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   N-[1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-pyrrolidin-3-yl]-acetamide; -   1-(1-Acetyl-3,3-dimethyl-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-propionamide; -   1-(5-tert-Butyl-2-methyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethanesulfonyl-phenyl)-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-isobutyramide; -   2-(4-tert-Butyl-2-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenoxy)-acetamide; -   1-(5-tert-Butyl-2-oxo-2,3-dihydro-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-3-cyano-2-methoxymethoxy-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-3-cyano-2-hydroxy-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-3-cyano-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(1,3,3-trimethyl-2,3-dihydro-1H-indol-5-yl)-urea; -   1-(5-tert-Butyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-benzenesulfonamide; -   Ethanesulfonic acid     (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   2,2,2-Trifluoro-ethanesulfonic acid     (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; -   N-(5-{4-[3-(5-tert-Butyl-2-methyl-phenyl)-ureido]-naphthalen-1-yl}-pyrazin-2-yl)-methanesulfonamide; -   1-[4-(6-{[Bis-(2-cyano-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-methyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-piperidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-tetrahydro-thiopyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(tetrahydro-pyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-(tetrahydro-furan-2-ylmethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methoxymethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-morpholin-4-yl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methyl-3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperidine-3-carboxylic     acid amide; -   1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperidine-4-carboxylic     acid amide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-114-thiomorpholin-4-ylmethyl)-pyridin-pg,120     3-yl]-naphthalen-1-yl}-urea; -   1-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-{4-[6-(4-Acetyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-3-(5-tert-butyl-2-methoxy-phenyl)-urea; -   4-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperazine-1-carboxylic     acid ethyl ester; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-pyridin-3-yl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(tetrahydro-furan-3-ylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-pyridin-3-ylmethyl-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-methylsulfanyl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-oxa-5-aza-bicyclo[2.2.1]hept-5-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-piperazin-1-yl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-pyrimidin-2-yl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-pyridin-2-yl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[4-(3-methoxy-phenyl)-piperazin-1-ylmethyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(morpholine-4-carbonyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-thia-5-aza-bicyclo[2.2.1]hept-5-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(5-morpholin-4-ylmethyl-pyrazin-2-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-yl)-acetamide; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-N-methyl-acetamide; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-2,2,2-trifluoro-acetamide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(pyridin-3-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(pyridin-3-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   [4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-carbamic     acid 3-tert-butyl-phenyl ester; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide     and     the pharmaceutically acceptable derivatives thereof.

In another embodiment of the invention there are provided the following compounds of formula (III) which are useful in the novel methods described herein:

-   1-(3-Methyl-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; -   1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,3-Dimethyl-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-{5-tert-Butyl-2-methyl-3-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(2,2-Dimethyl-propionyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(3-hydroxy-prop-1-ynyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-2-(3-hydroxy-prop-1-ynyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butoxy-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-(1-Cyano-cyclopropyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[5-tert-Butyl-3-(2-diethylamino-ethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-[1,3]dioxolan-2-yl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-pyrrolidin-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-dimethylamino-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-propoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-hydroxymethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-Cyclohexyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2,4-Dimethoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-methyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-Acetyl-N-(5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; -   1-(6-tert-Butyl-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-isopropoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-imidazol-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-3-ethylamino-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-bis(methanesulfon)amide; -   1-[5-tert-Butyl-2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(2-Methanesulfinyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-{[Bis-(2-methoxy-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; -   N-[1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-pyrrolidin-3-yl]-acetamide; -   1-(1-Acetyl-3,3-dimethyl-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-propionamide; -   1-(5-tert-Butyl-2-methyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethanesulfonyl-phenyl)-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-isobutyramide; -   2-(4-tert-Butyl-2-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenoxy)-acetamide; -   1-(5-tert-Butyl-2-oxo-2,3-dihydro-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-3-cyano-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-benzenesulfonamide; -   Ethanesulfonic acid     (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   2,2,2-Trifluoro-ethanesulfonic acid     (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; -   N-(5-{4-[3-(5-tert-Butyl-2-methyl-phenyl)-ureido]-naphthalen-1-yl}-pyrazin-2-yl)-methanesulfonamide; -   1-[4-(6-{[Bis-(2-cyano-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-methyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-piperidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-tetrahydro-thiopyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(tetrahydro-pyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-(tetrahydro-furan-2-ylmethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methoxymethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methyl-3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperidine-3-carboxylic     acid amide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-114-thiomorpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(tetrahydro-furan-3-ylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-pyridin-3-ylmethyl-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-oxa-5-aza-bicyclo[2.2.1]hept-5-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[4-(3-methoxy-phenyl)-piperazin-1-ylmethyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(morpholine-4-carbonyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(5-morpholin-4-ylmethyl-pyrazin-2-yl)-naphthalen-1-yl]-urea; -   1-(6-tert-Butyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-yl)-acetamide; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-N-methyl-acetamide; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-2,2,2-trifluoro-acetamide; -   1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(pyridin-3-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; -   [4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-carbamic     acid 3-tert-butyl-phenyl ester; -   N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide     and     the pharmaceutically acceptable derivatives thereof.

In addtion to the abovementioned compounds the following prophetic compounds of the formula (III) may be useful in the novel methods described herein:

-   1-(5-tert-Butyl-2-methylsulfanyl-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-chloro-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   1-(5-tert-Butyl-2-methylamino-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; -   N-(5-tert-Butyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-2-oxo-2H-pyridin-1-yl)-methanesulfonamide; -   5-tert-Butyl-7-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzooxazole-2-carboxylic     acid amide; -   2-(5-tert-Butyl-7-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzooxazol-2-yl)-acetamide; -   5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzamide     and     the pharmaceutically acceptable derivatives thereof.

The invention includes the use of any compounds of described above containing one or more asymmetric carbon atoms may occur as racemates and racemic mixtures, single enantiomers, diastereomeric mixtures and individual diastereomers. All such isomeric forms of these compounds are expressly included in the present invention. Each stereogenic carbon may be in the R or S configuration, or a combination of configurations.

Some of the compounds of formulas (I), (Ia), (II) and (III) can exist in more than one tautomeric form. The invention includes methods using all such tautomers.

All terms as used herein in this specification, unless otherwise stated, shall be understood in their ordinary meaning as known in the art. For example, “C₁₋₄alkoxy” is a C₁₋₄alkyl with a terminal oxygen, such as methoxy, ethoxy, propoxy, pentoxy and hexoxy. All alkyl, alkenyl and alkynyl groups shall be understood as being branched or unbranched where structurally possible and unless otherwise specified. Other more specific definitions are as follows:

The term “aroyl” as used in the present specification shall be understood to mean “benzoyl” or “naphthoyl”.

The term “carbocycle” shall be understood to mean an aliphatic hydrocarbon radical containing from three to twelve carbon atoms. Carbocycles include hydrocarbon rings containing from three to ten carbon atoms. These carbocycles may be either aromatic and non-aromatic ring systems. The non-aromatic ring systems may be mono- or polyunsaturated. Preferred carbocycles include but are not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptanyl, cycloheptenyl, phenyl, indanyl, indenyl, benzocyclobutanyl, dihydronaphthyl, tetrahydronaphthyl, naphthyl, decahydronaphthyl, benzocycloheptanyl and benzocycloheptenyl. Certain terms for cycloalkyl such as cyclobutanyl and cyclobutyl shall be used inerchangeably.

The term “heterocycle” refers to a stable nonaromatic 4-8 membered (but preferably, 5 or 6 membered) monocyclic or nonaromatic 8-11 membered bicyclic heterocycle radical which may be either saturated or unsaturated. Each heterocycle consists of carbon atoms and one or more, preferably from 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur. The heterocycle may be attached by any atom of the cycle, which results in the creation of a stable structure. Unless otherwise stated, heterocycles include but are not limited to, for example oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, piperidinyl, piperazinyl, morpholinyl, tetrahydropyranyl, dioxanyl, tetramethylene sulfonyl, tetramethylene sulfoxidyl, oxazolinyl, thiazolinyl, imidazolinyl, tertrahydropyridinyl, homopiperidinyl, pyrrolinyl, tetrahydropyrimidinyl, decahydroquinolinyl, decahydroisoquinolinyl, thiomorpholinyl, thiazolidinyl, dihydrooxazinyl, dihydropyranyl, oxocanyl, heptacanyl, thioxanyl, dithianyl or 2-oxa- or 2-thia-5-aza-bicyclo[2.2.1]heptanyl.

The term “heteroaryl” shall be understood to mean an aromatic 5-8 membered monocyclic or 8-11 membered bicyclic ring containing 1-4 heteroatoms such as N,O and S. Unless otherwise stated, such heteroaryls include: pyridinyl, pyridonyl, quinolinyl, dihydroquinolinyl, tetrahydroquinoyl, isoquinolinyl, tetrahydroisoquinoyl, pyridazinyl, pyrimidinyl, pyrazinyl, benzimidazolyl, benzthiazolyl, benzoxazolyl, benzofuranyl, benzothiophenyl, benzpyrazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, benzooxazolonyl, benzo[1,4]oxazin-3-onyl, benzodioxolyl, benzo[1,3]dioxol-2-onyl, tetrahydrobenzopyranyl, indolyl, indolinyl, indolonyl, indolinonyl, phthalimidyl.

The invention includes methods of using pharmaceutically acceptable derivatives of compounds of formula (I), (Ia), (II) and (III). A “pharmaceutically acceptable derivative” refers to any pharmaceutically acceptable salt or ester, or any other compound which, upon administration to a patient, is capable of providing (directly or indirectly) a compound useful for the invention, or a pharmacologically active metabolite or pharmacologically active residue thereof. A pharmacologically active metabolite shall be understood to mean any compound of the invention capable of being metabolized enzymatically or chemically. This includes, for example, hydroxylated or oxidized derivative compounds of the formulas (I), (Ia), (II) or (III).

Pharmaceutically acceptable salts include those derived from pharmaceutically acceptable inorganic and organic acids and bases. Examples of suitable acids include hydrochloric, hydrobromic, sulfuric, nitric, perchloric, fumaric, maleic, phosphoric, glycolic, lactic, salicylic, succinic, toluene-p-sulfuric, tartaric, acetic, citric, methanesulfonic, formic, benzoic, malonic, naphthalene-2-sulfuric and benzenesulfonic acids. Other acids, such as oxalic acid, while not themselves pharmaceutically acceptable, may be employed in the preparation of salts useful as intermediates in obtaining the compounds and their pharmaceutically acceptable acid addition salts. Salts derived from appropriate bases include alkali metal (e.g., sodium), alkaline earth metal (e.g., magnesium), ammonium and N—(C₁-C₄ alkyl)₄ ⁺ salts.

In addition, within the scope of the invention is use of prodrugs of compounds of the formula (I), (Ia), (II) and (III). Prodrugs include those compounds that, upon simple chemical transformation, are modified to produce compounds of the invention. Simple chemical transformations include hydrolysis, oxidation and reduction. Specifically, when a prodrug is administered to a patient, the prodrug may be transformed into a compound disclosed hereinabove, thereby imparting the desired pharmacological effect.

Methods of Use

In accordance with the invention, there are provided novel methods of using the compounds of the formulas (I), (Ia), (II) and (III). as described in WO 00/55139 and U.S. application Ser. No. 09/505,582. The compounds disclosed therein effectively block inflammatory cytokine production from cells. The inhibition of cytokine production is an attractive means for preventing and treating a variety of cytokine mediated diseases or conditions associated with excess cytokine production, e.g., diseases and pathological conditions involving inflammation. Thus, the compounds are described in WO 00/55139 as being useful for the treatment of the following conditions and diseases: osteoarthritis, multiple sclerosis, Guillain-Barre syndrome, Crohn's disease, ulcerative colitis, psoriasis, graft versus host disease, systemic lupus erythematosus and insulin-dependent diabetes mellitus, rheumatoid arthritis, Alzheimer's disease, toxic shock syndrome, diabetes, inflammatory bowel diseases, acute and chronic pain as well as symptoms of inflammation and cardiovascular disease, stroke, myocardial infarction, alone or following thrombolytic therapy, thermal injury, adult respiratory distress syndrome (ARDS), multiple organ injury secondary to trauma, acute glomerulonephritis, dermatoses with acute inflammatory components, acute purulent meningitis or other central nervous system disorders, hemodialysis, leukopherisis, granulocyte transfusion associated syndromes, and necrotizing entrerocolitis.

Suprisingly, it has been discovered for the first time that the compounds disclosed in WO 00/55139 are useful in methods for treating: acute and chronic inflammation in the lung caused by inhalation of smoke, endometriosis, Behcet's disease, uveitis, ankylosing spondylitis, pancreatitis, cancer, Lyme disease, restenosis following percutaneous transluminal coronary angioplasty, Alzheimer's disease, traumatic arthritis, sepsis, chronic obstructive pulmonary disease and congestive heart failure.

For therapeutic use, the compounds may be administered in any conventional dosage form in any conventional manner. Routes of administration include, but are not limited to, intravenously, intramuscularly, subcutaneously, intrasynovially, by infusion, sublingually, transdermally, orally, topically or by inhalation. The preferred modes of administration are oral and intravenous.

The compounds may be administered alone or in combination with adjuvants that enhance stability of the inhibitors, facilitate administration of pharmaceutic compositions containing them in certain embodiments, provide increased dissolution or dispersion, increase inhibitory activity, provide adjunct therapy, and the like, including other active ingredients. Advantageously, such combination therapies utilize lower dosages of the conventional therapeutics, thus avoiding possible toxicity and adverse side effects incurred when those agents are used as monotherapies. The above described compounds may be physically combined with the conventional therapeutics or other adjuvants into a single pharmaceutical composition. Reference is this regard may be made to Cappola et al.: U.S. patent application Ser. No. 09/902,822 and PCT/US 01/21860 each incorporated by reference herein in their entirety. Advantageously, the compounds may then be administered together in a single dosage form. In some embodiments, the pharmaceutical compositions comprising such combinations of compounds contain at least about 5%, but more preferably at least about 20%, of a compound of formulas (I), (Ia), (II) and (III) (w/w) or a combination thereof. The optimum percentage (w/w) of a compound of the invention may vary and is within the purview of those skilled in the art. Alternatively, the compounds may be administered separately (either serially or in parallel). Separate dosing allows for greater flexibility in the dosing regime.

As mentioned above, dosage forms of the compounds described herein include pharmaceutically acceptable carriers and adjuvants known to those of ordinary skill in the art. These carriers and adjuvants include, for example, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, buffer substances, water, salts or electrolytes and cellulose-based substances. Preferred dosage forms include, tablet, capsule, caplet, liquid, solution, suspension, emulsion, lozenges, syrup, reconstitutable powder, granule, suppository and transdermal patch. Methods for preparing such dosage forms are known (see, for example, H. C. Ansel and N. G. Popovish, Pharmaceutical Dosage Forms and Drug Delivery Systems, 5th ed., Lea and Febiger (1990)). Dosage levels and requirements are well-recognized in the art and may be selected by those of ordinary skill in the art from available methods and techniques suitable for a particular patient. In some embodiments, dosage levels range from about 1-1000 mg/dose for a 70 kg patient. Although one dose per day may be sufficient, up to 5 doses per day may be given. For oral doses, up to 2000 mg/day may be required. As the skilled artisan will appreciate, lower or higher doses may be required depending on particular factors. For instance, specific dosage and treatment regimens will depend on factors such as the patient's general health profile, the severity and course of the patient's disorder or disposition thereto, and the judgment of the treating physician.

General Synthetic Methods

The compounds described hereinabove may be prepared by Method A, B, or C as illustrated in Scheme I, preferably method C, in WO 00/55139. Starting materials used are either commercially available or easily prepared from commercially available materials known by those skilled in the art. Further reference in this regard may be made to U.S. application Ser. Nos. 09/505,582, 09/484,638, 09/714,539, 09/611,109, 09/698,442 and U.S. provisional application No. 60/216,283. Each of the aforementioned incorporated herein by reference in their entirety.

Assessment of Biolocical Properties

Inhibition of TNF Production in THP Cells

The inhibition of cytokine production can be observed by measuring inhibition of TNFα in lipopolysaccharide stimulated THP cells (for example, see W. Prichett et al., 1995, J Inflammation, 45, 97). All cells and reagents were diluted in RPMI 1640 with phenol red and L-glutamine, supplemented with additional L-glutamine (total: 4 mM), penicillin and streptomycin (50 units/ml each) and fetal bovine serum (FBS, 3%) (GIBCO, all conc. final). Assay was performed under sterile conditions; only test compound preparation was nonsterile. Initial stock solutions were made in DMSO followed by dilution into RPMI 1640 2-fold higher than the desired final assay concentration. Confluent THP.1 cells (2×10⁶ cells/ml, final conc.; American Type Culture Company, Rockville, Md.) were added to 96 well polypropylene round bottomed culture plates (Costar 3790; sterile) containing 125 μl test compound (2 fold concentrated) or DMSO vehicle (controls, blanks). DMSO concentration did not exceed 0.2% final. Cell mixture was allowed to preincubate for 30 min, 37° C., 5% CO₂ prior to stimulation with lipopolysaccharide (LPS; 1 μg/ml final; Siga L-2630, from E.coli serotype 0111. B4; stored as 1 mg/ml stock in endotoxin screened distilled H₂O at −80° C.). Blanks (unstimulated) received H₂O vehicle; final incubation volume was 250 μl. Overnight incubation (18-24 hr) proceeded as described above. Assay was terminated by centrifuging plates 5 min, room temperature, 1600 rpm (400×g); supernatants were transferred to clean 96 well plates and stored −80° C. until analyzed for human TNFα by a commercially available ELISA kit (Biosource #KHC3015, Camarillo, Calif.). Data was analyzed by non-linear regression (Hill equation) to generate a dose response curve using SAS Software System (SAS institute, Inc., Cary, NC). The calculated IC50 value is the concentration of the test compound that caused a 50% decrease in the maximal TNFα production.

Preferred compounds including those from the synthetic examples above were evaluated and had IC₅₀<10 uM in this assay.

Inhibition of Other Cytokines

By similar methods using peripheral blood monocytic cells, appropriate stimuli, and commercially available ELISA kits (or other method of detection such as radioimmunoassay), for a particular cytokine, inhibition of IL-1beta, GM-CSF, IL-6 and IL-8 can be demonstrated for preferred compounds (for example, see J. C. Lee et al., 1988, Int. J. Immunopharmacol., 10,835). 

1. A method of treating cancer, said method comprising administering to a patient a therapeutically effective amount of a compound of the formula (III):

wherein: E is carbon or a heteroatom group chosen from —O—, —NH— and —S—; G is: an aromatic C₆₋₁₀ carbocycle or a nonaromatic C₃₋₁₀carbocycle saturated or unsaturated; a 6-14 membered monocyclic, bicyclic or tricyclic heteroaryl containing 1 or more heteroatoms chosen from O, N and S; a 6-8 membered monocyclic heterocycle containing one or more heteroatoms chosen from O, N and S; or an 8-11 membered bicyclic heterocycle, containing one or more heteroatoms chosen from O, N and S; wherein G is optionally substituted by one or more R₁, R₂ or R₃; Ar is: phenyl, naphthyl, quinolinyl, isoquinolinyl, tetrahydronaphthyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, benzimidazolyl, benzofuranyl, dihydrobenzofuranyl, indolinyl, benzothienyl, dihydrobenzothienyl, indanyl, indenyl or indolyl each being optionally substituted by one or more R₄ or R₅; X is: a C₅₋₈ cycloalkyl or cycloalkenyl optionally substituted with one to two oxo groups or one to three C₁₋₄ alkyl, C₁₋₄ alkoxy or C₁₋₄ alkylamino chains each being branched or unbranched; aryl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, pyridinyl, pyrimidinyl, pyridinonyl, dihydropyridinonyl, maleimidyl, dihydromaleimidyl, piperdinyl, benzimidazole, 3H-imidazo[4,5-b]pyridine, piperazinyl, pyridazinyl or pyrazinyl; each being optionally independently substituted with one to three C₁₋₄ alkyl, C₁₋₄alkoxy, hydroxy, nitrile, amino, mono- or di-(C₁₋₃ alkyl)amino, mono- or di-(C₁₋₃ alkylamino)carbonyl, NH₂C(O), C₁₋₆ alkyl-S(O)_(m) or halogen; Y is: a bond or a C₁₋₄ saturated or unsaturated branched or unbranched carbon chain optionally partially or fully halogenated, wherein one or more C atoms are optionally replaced by O, N, or S(O)_(m) and wherein Y is optionally independently substituted with one to two oxo groups, nitrile, phenyl or one or more C₁₋₄ alkyl optionally substituted by one or more halogen atoms; Z is: aryl, heteroaryl selected from pyridinyl, piperazinyl, pyrimidinyl, pyridazinyl, pyrazinyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, furanyl, thienyl and pyranyl, heterocycle selected from tetrahydropyrimidonyl, cyclohexanonyl, cyclohexanolyl, 2-oxa- or 2-thia-5-aza-bicyclo[2.2.1]heptanyl, pentamethylene sulfidyl, pentamethylene sulfoxidyl, pentamethylene sulfonyl, tetramethylene sulfidyl, tetramethylene sulfoxidyl or tetramethylene sulfonyl, tetrahydropyranyl, tetrahydrofuranyl, 1,3-dioxolanonyl, 1,3-dioxanonyl, 1,4-dioxanyl, morpholino, thiomorpholino, thiomorpholino sulfoxidyl, thiomorpholino sulfonyl, piperidinyl, piperidinonyl, pyrrolidinyl and dioxolanyl, each of the aforementioned Z are optionally substituted with one to three halogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₁₋₃ alkoxy-C₁₋₃ alkyl, C₁₋₆ alkoxycarbonyl, aroyl, C₁₋₃acyl, oxo, hydroxy, pyridinyl-C₁₋₃ alkyl, imidazolyl-C₁₋₃ alkyl, tetrahydrofuranyl-C₁₋₃ alkyl, nitrile-C₁₋₃ alkyl, nitrile, carboxy, phenyl wherein the phenyl ring is optionally substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or mono- or di-(C₁₋₃ alkyl)amino, C₁₋₆ alkyl-S(O)_(m), or phenyl-S(O)_(m) wherein the phenyl ring is optionally substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy, halogen or mono- or di-(C₁₋₃ alkyl)amino; or Z is optionally substituted with one to three amino or amino-C₁₋₃ alkyl wherein the N atom is optionally independently mono- or di-substituted by aminoC₁₋₆alkyl, C₁₋₃alkyl, arylC₀₋₃alkyl, C₁₋₅ alkoxyC₁₋₃ alkyl, C₁₋₅ alkoxy, aroyl, C₁₋₃acyl, C₁₋₃alkyl-S(O)_(m)— or arylC₀₋₃alkyl-S(O)_(m)— each of the aforementioned alkyl and aryl attached to the amino group is optionally substituted with one to two halogen, C₁₋₆ alkyl or C₁₋₆ alkoxy; or Z is optionally substituted with one to three aryl, heterocycle or heteroaryl as hereinabove described in this paragraph each in turn is optionally substituted by halogen, C₁₋₆ alkyl or C₁₋₆ alkoxy; or Z is hydroxy, halogen, nitrile, amino wherein the N atom is optionally independently mono- or di-substituted by C₁₋₃acyl, C₁₋₆alkyl or C₁₋₃alkoxyC₁₋₃alkyl, C₁₋₆alkyl branched or unbranched, C₁₋₆alkoxy, C₁₋₃acylamino, nitrileC₁₋₄ alkyl, C₁₋₆ alkyl-S(O)_(m), and phenyl-S(O)_(m), wherein the phenyl ring is optionally substituted with one to two halogen, C₁₋₆ alkoxy, hydroxy or mono- or di-(C₁₋₃ alkyl)amino; each R₁ is independently: C₁₋₁₀ alkyl branched or unbranched optionally partially or fully halogenated, wherein one or more C atoms are optionally independently replaced by O, N or S(O)_(m), and wherein said C₁₋₁₀ alkyl is optionally substituted with one to three C₃₋₁₀ cycloalkyl, hydroxy, oxo, phenyl, naphthyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, pyrrolidinyl, imidazolyl, pyrazolyl, thienyl, furyl, dioxolanyl, isoxazolyl or isothiazolyl; each of the aforementioned being optionally substituted with one to five groups selected from halogen, C₁₋₆ alkyl which is optionally partially or fully halogenated, C₃₋₈ cycloalkanyl, C₅₋₈ cycloalkenyl, hydroxy, nitrile, C₁₋₃ alkoxy which is optionally partially or fully halogenated or NH₂C(O), mono- or di(C₁₋₃ alkyl)amino, and mono- or di(C₁₋₃alkyl)aminocarbonyl; or R₁ is cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, or cycloheptyloxy each being optionally partially or fully halogenated and optionally substituted with one to three C₁₋₃ alkyl groups optionally partially or fully halogenated, nitrile, hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloalkyl group wherein one to three ring methylene groups are independently replaced by O, S(O)_(m), CHOH, >C═O, >C═S or NH; phenyloxy or benzyloxy each being optionally partially or fully halogenated and optionally substituted with one to three C₁₋₃ alkyl groups optionally partially or fully halogenated, nitrile, hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloaryl group wherein one to two ring methyne groups are independently replaced by N; cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, bicyclopentanyl, bicyclohexanyl or bicycloheptanyl, each being optionally partially or fully halogenated and optionally substituted with one to three C₁₋₃ alkyl optionally partially or fully halogenated, nitrile, hydroxyC₁₋₃alkyl or aryl; or an analog of such cycloalkyl group wherein one to three ring methylene groups are independently replaced by O, S(O)_(m), CHOH, >C═O, >C═S or NH; C₃₋₁₀ branched or unbranced alkenyl each being optionally partially or fully halogenated, and optionally substituted with one to three C₁₋₅ branched or unbranched alkyl, phenyl, naphthyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl or isothiazolyl, each of the aforementioned being substituted with one to five halogen, C₁₋₆ alkyl which is optionally partially or fully halogenated, cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl and bicycloheptanyl, hydroxy, nitrile, C₁₋₃ alkyloxy which is optionally partially or fully halogenated, NH₂C(O), mono- or diC₁₋₃alkyl)aminocarbonyl; the C₃₋₁₀ branched or unbranced alkenyl being optionally interrupted by one or more heteroatoms chosen from O, N and S(O)_(m); cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl, cycloheptadienyl, bicyclohexenyl or bicycloheptenyl, wherein such cycloalkenyl group is optionally substituted with one to three C₁₋₃ alkyl groups; oxo, nitrile, halogen; silyl containing three C₁₋₄ alkyl groups optionally partially or fully halogenated; or C₃₋₆ alkynyl branched or unbranched carbon chain optionally partially or fully halogenated, wherein one or more methylene groups are optionally replaced by O, NH or S(O)_(m) and wherein said alkynyl group is optionally independently substituted with one to two oxo groups, hydroxy, pyrroldinyl, pyrrolyl, tetrahydropyranyl, one or more C₁₋₄ alkyl optionally substituted by one or more halogen atoms, nitrile, morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono- or di(C₁₋₃alkyl)amino optionally substituted by one or more halogen atoms; each R₂, R₄, and R₅ is a C₁₋₆ branched or unbranched alkyl optionally partially or fully halogenated, C₁₋₆acyl, aroyl, C₁₋₄ branched or unbranched alkoxy, each being optionally partially or fully halogenated, halogen, methoxycarbonyl, C₁₋₃ alkyl-S(O)_(m) optionally partially or fully halogenated, or phenyl-S(O)_(m); OR₆, C₁₋₆ alkoxy, hydroxy, nitrile, nitro, halogen; or amino-S(O)_(m)— wherein the N atom is optionally independently mono- or di-substituted by C₁₋₆alkyl or arylC₀₋₃alkyl, or amino wherein the N atom is optionally independently mono- or di-substituted by C₁₋₃alkyl, arylC₀₋₃alkyl, C₁₋₆acyl, C₁₋₆alkyl-S(O)_(m)— or arylC₀₋₃alkyl-S(O)_(m)—, each of the aforementioned alkyl and aryl in this subparagraph are optionally partially or fully halogenated and optionally substituted with one to two C₁₋₆ alkyl or C₁₋₆ alkoxy; each R₃ is independently: phenyl, naphthyl, morpholino, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, pyrrolidinyl, imidazolyl, pyrazolyl, thiazolyl, oxazoyl, [1,3,4]oxadiazol, triazolyl, tetrazolyl, thienyl, furyl, tetrahydrofuryl, isoxazolyl, isothiazolyl, quinolinyl, isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl, benzoxazolyl, benzisoxazolyl, benzpyrazolyl, benzothiofuranyl, cinnolinyl, pterindinyl, phthalazinyl, naphthypyridinyl, quinoxalinyl, quinazolinyl, purinyl or indazolyl, each of the aforementioned is optionally substituted with one to three phenyl, naphthyl, heterocycle or heteroaryl as hereinabove described in this paragraph, C₁₋₆ branched or unbranched alkyl which is optionally partially or fully halogenated, cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl, bicycloheptanyl, phenyl C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl, halogen, hydroxy, oxo, nitrile, C₁₋₃ alkoxy optionally partially or fully halogenated, phenyloxy, naphthyloxy, heteroaryloxy or heterocyclicoxy wherein the heterocyclic or heteroaryl moiety is as hereinabove described in this paragraph, nitro, amino, mono- or di-(C₁₋₃alky)lamino, phenylamino, naphthylamino, heteroaryl or heterocyclic amino wherein the heteroaryl heterocyclic moiety is as hereinabove described in this paragraph, NH₂C(O), a mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl, amino-C₁₋₅ alkyl, mono- or di-(C₁₋₅alkyl)amino, mono- or di-(C₁₋₃alkyl)amino-C₁₋₅ alkyl, amino-S(O)₂, di-(C₁₋₃alkyl)amino-S(O)₂, R₇—C₁₋₅ alkyl, R₈—C₁₋₅ alkoxy, R₉—C(O)—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkyl(R₁₁)N, carboxy-mono- or di-(C₁₋₅alkyl)-amino; a fused aryl selected from benzocyclobutanyl, indanyl, indenyl, dihydronaphthyl, tetrahydronaphthyl, benzocycloheptanyl and benzocycloheptenyl, or a fused heteroaryl selected from cyclopentenopyridinyl, cyclohexanopyridinyl, cyclopentanopyrimidinyl, cyclohexanopyrimidinyl, cyclopentanopyrazinyl, cyclohexanopyrazinyl, cyclopentanopyridazinyl, cyclohexanopyridazinyl, cyclopentanoquinolinyl, cyclohexanoquinolinyl, cyclopentanoisoquinolinyl, cyclohexanoisoquinolinyl, cyclopentanoindolyl, cyclohexanoindolyl, cyclopentanobenzimidazolyl, cyclohexanobenzimidazolyl, cyclopentanobenzoxazolyl, cyclohexanobenzoxazolyl, cyclopentanoimidazolyl, cyclohexanoimidazolyl, cyclopentanothienyl and cyclohexanothienyl; wherein the fused aryl or fused heteroaryl ring is independently substituted with zero to three phenyl, naphthyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, pyrazolyl, thienyl, furyl, isoxazolyl, isothiazolyl, C₁₋₆ alkyl which is optionally partially or fully halogenated, halogen, nitrile, C₁₋₃ alkyloxy which is optionally partially or fully halogenated, phenyloxy, naphthyloxy, heteroaryloxy or heterocyclicoxy wherein the heteroaryl or heterocyclic moiety is as hereinabove described in this paragraph, nitro, amino, mono- or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl or heterocyclic amino wherein the heteroaryl or heterocyclic moiety is as hereinabove described in this paragraph, NH₂C(O), mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₄ alkyl-OC(O), C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl, amino-C₁₋₅ alkyl, mono- or di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, R₁₂—C₁₋₅ alkyl, R₁₃—C₁₋₅ alkoxy, R₁₄—C(O)—C₁₋₅ alkyl or R₁₅—C₁₋₅ alkyl(R₁₆)N; cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl or bicycloheptanyl, each being optionally be partially or fully halogenated and optionally substituted with one to three C₁₋₃ alkyl groups, or an analog of such cycloalkyl group wherein one to three ring methylene groups are independently replaced by O, S, CHOH, >C═O, >C═S or NH; cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl, cycloheptadienyl, bicyclohexenyl or bicycloheptenyl, each optionally substituted with one to three C₁₋₃ alkyl groups; C₁₋₄ alkyl-phenyl-C(O)—C₁₋₄ alkyl-, C₁₋₄ alkyl-C(O)—C₁₋₄ alkyl- or C₁₋₄ alkyl-phenyl-S(O)_(m)—C₁₋₄ alkyl-; C₁₋₆ alkyl or C₁₋₆ branched or unbranched alkoxy each of which is optionally partially or fully halogenated or optionally substituted with R₁₇; OR₁₈ or C₁₋₆ alkyl optionally substituted with OR₁₈; amino or mono- or di-(C₁₋₅alkyl)amino optionally substituted with R₁₉; R₂₀C(O)N(R₂₁)—, R₂₂O— or R₂₃R₂₄NC(O)—; R₂₆(CH₂)_(m)C(O)N(R₂₁)—, R₂₃R₂₄NC(O)—C₁₋₃alkoxy or R₂₆C(O)(CH₂)_(m)N(R₂₁)—; C₂₋₆alkenyl substituted by R₂₃R₂₄NC(O)—; C₂₋₆ alkynyl branched or unbranched carbon chain, optionally partially or fully halogenated, wherein one or more methylene groups are optionally replaced by O, NH, S(O)_(m) and wherein said alkynyl group is optionally independently substituted with one to two oxo groups, pyrroldinyl, pyrrolyl, morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl one or more C₁₋₄ alkyl optionally substituted by one or more halogen atoms, nitrile, morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono- or di(C₁₋₄ alkyl)amino optionally substituted by one or more halogen atoms; C₁₋₆acyl or aroyl; R₆ is a: C₁₋₄ alkyl optionally partially or fully halogenated and optionally substituted with R₂₆; each R₇, R₈, R₉, R₁₀, R₁₂, R₁₃, R₁₄, R₁₅, R₁₇, R₁₉, R₂₅ and R₂₆ is independently: nitrile, phenyl, morpholino, piperidinyl, piperazinyl, imidazolyl, pyridinyl, tetrazolyl, amino or mono- or di-(C₁₋₄alkyl)amino optionally partially or fully halogenated; each R₁₁ and R₁₆ is independently: hydrogen or C₁₋₄ alkyl optionally partially or fully halogenated; R₁₈ is independently: hydrogen or a C₁₋₄ alkyl optionally independently substituted with oxo or R₂₅; R₂₀ is independently: C₁₋₁₀ alkyl optionally partially or fully halogenated, phenyl, or pyridinyl; R₂₁ is independently: hydrogen or C₁₋₃ alkyl optionally partially or fully halogenated; each R₂₂, R₂₃ and R₂₄ is independently: hydrogen, C₁₋₆ alkyl optionally partially or fully halogenated, said C₁₋₆ alkyl is optionally interrupted by one or more O, N or S, said C₁₋₆ alkyl also being independently optionally substituted by mono- or di-(C₁₋₃alkyl)aminocarbonyl, phenyl, pyridinyl, amino or mono- or di-(C₁₋₄alkyl)amino each of which is optionally partially or fully halogenated and optionally substituted with mono- or di-(C₁₋₃alkyl)amino; or R₂₃ and R₂₄ taken together optionally form a heterocyclic or heteroaryl ring; m=0, 1 or 2; W is O or S and the pharmaceutically acceptable salts thereof.
 2. The method according to claim 1 wherein E is —CH₂—, —NH— or —O—; W is O; and G is: phenyl, naphthyl, benzocyclobutanyl, dihydronaphthyl, tetrahydronaphthyl, benzocycloheptanyl, benzocycloheptenyl, indanyl, indenyl; pyridinyl, pyridonyl, quinolinyl, dihydroquinolinyl, tetrahydroquinoyl, isoquinolinyl, tetrahydroisoquinoyl, pyridazinyl, pyrimidinyl, pyrazinyl, benzimidazolyl, benzthiazolyl, benzooxazolyl, benzofuranyl, benzothiophenyl, benzpyrazolyl, dihydrobenzofuranyl, dibenzofuranyl, dihydrobenzothiophenyl, benzooxazolonyl, benzo[1,4]oxazin-3-onyl, benzodioxolyl, benzo[1,3]dioxol-2-onyl, benzofuran-3-onyl, tetrahydrobenzopyranyl, indolyl, 2,3-dihydro-1H-indolyl, indolinyl, indolonyl, indolinonyl, phthalimidyl, chromoyl; oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, piperidinyl, piperazinyl, morpholino, tetrahydropyranyl, dioxanyl, tetramethylene sulfonyl, tetramethylene sulfoxidyl, oxazolinyl, 3,4-dihydro-2H-benzo[1,4]oxazinyl, thiazolinyl, imidazolinyl, tertrahydropyridinyl, homopiperidinyl, pyrrolinyl, tetrahydropyrimidinyl, decahydroquinolinyl, decahydroisoquinolinyl, thiomorpholino, thiazolidinyl, dihydrooxazinyl, dihydropyranyl, oxocanyl, heptacanyl, thioxanyl or dithianyl; wherein G is optionally substituted by one or more R₁, R₂ or R₃.
 3. The method according to claim 2 wherein E is —NH—; G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl, isoquinolinyl, pyrazinyl, benzimidazolyl, benzooxazolyl, benzooxazolonyl, benzofuranyl, benzothiophenyl, benzpyrazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, 3,4-dihydro-2H-benzo[1,4]oxazinyl, indanyl, indenyl, indolyl, indolinyl, indolonyl, 2,3-dihydro-1H-indolyl or indolinonyl, wherein G is optionally substituted by one or more R₁, R₂ or R₃; Ar is: naphthyl, quinolinyl, isoquinolinyl, tetrahydronaphthyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, indanyl, indenyl or indolyl each being optionally substituted by one or more R₄ or R₅ groups; X is: phenyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, pyridinyl, pyrimidinyl, pyridinonyl, dihydropyridinonyl, maleimidyl, dihydromaleimidyl, piperdinyl, piperazinyl, pyridazinyl or pyrazinyl; each being optionally independently substituted with one to three C₁₋₄ alkyl, C₁₋₄alkoxy, hydroxy, nitrile, amino, mono- or di-(C₁₋₃ alkyl)amino, mono- or di-(C₁₋₃ alkylamino)carbonyl, NH₂C(O), C₁₋₆ alkyl-S(O)_(m) or halogen; Y is: a bond or a C₁₋₄ saturated or unsaturated carbon chain wherein one or more of the C atoms is optionally replaced by O, N, or S(O)_(m) and wherein Y is optionally independently substituted with one to two oxo groups, nitrile, phenyl or one or more C₁₋₄ alkyl optionally substituted by one or more halogen atoms; Z is: phenyl, heteroaryl selected from pyridinyl, piperazinyl, pyrimidinyl, pyridazinyl, pyrazinyl, imidazolyl, furanyl, thienyl and pyranyl, heterocycle selected from 2-oxa-5-aza-bicyclo[2.2.1]heptanyl, tetrahydropyrimidonyl, pentamethylene sulfidyl, pentamethylene sulfoxidyl, pentamethylene sulfonyl, tetramethylene sulfidyl, tetramethylene sulfoxidyl tetramethylene sulfonyl, tetrahydropyranyl, tetrahydrofuranyl, 1,3-dioxolanonyl, 1,3-dioxanonyl, 1,4-dioxanyl, morpholino, thiomorpholino, thiomorpholino sulfoxidyl, piperidinyl, piperidinonyl, dihydrothiazolyl, dihydrothiazolyl sulfoxidyl, pyrrolidinyl and dioxolanyl which are optionally substituted with one to three nitrile, C₁₋₃ alkyl, C₁₋₃ alkoxy, amino, mono- or di-(C₁₋₃ alkyl)amino, CONH₂ or OH; or Z is optionally substituted by phenyl, heterocycle or heteroaryl as hereinabove described in this paragraph each in turn is optionally substituted by halogen, C₁₋₃ alkyl or C₁₋₃ alkoxy; or Z is nitrile, nitrileC₁₋₃ alkyl, C₁₋₆ alkyl-S(O)_(m), halogen, hydroxy, C₁₋₃ alkyl, C₁₋₃ acylamino, C₁₋₄ alkoxy, amino, mono- or di-(C₁₋₃ alkyl)aminocarbonyl, or amino mono or di-substituted by aminoC₁₋₆ alkyl or C₁₋₃alkoxyC₁₋₃alkyl; each R₁ is independently: C₁₋₆ alkyl branched or unbranched optionally partially or fully halogenated, wherein one or more C atoms are optionally independently replaced by O, N or S(O)_(m), and wherein said C₁₋₆ alkyl is optionally substituted with one to three C₃₋₆cycloalkyl, oxo, phenyl, dioxolanyl, pyrrolidinyl, furyl, isoxazolyl or isothiazolyl; each of the aforementioned being optionally substituted with one to three groups selected from halogen, C₁₋₃ alkyl which is optionally partially or fully halogenated, hydroxy, nitrile and C₁₋₃alkoxy which is optionally partially or fully halogenated; cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, bicyclopentanyl or bicyclohexanyl, each being optionally partially or fully halogenated and optionally substituted with one to three C₁₋₃ alkyl groups optionally partially or fully halogenated, nitrile, hydroxyC₁₋₃alkyl or phenyl; or an analog of such cycloalkyl group wherein one to three ring methylene groups are independently replaced by O, S, CHOH, >C═O, >C═S or NH; oxo; C₃₋₆ alkynyl branched or unbranched carbon chain optionally partially or fully halogenated, wherein one or more methylene groups are optionally replaced by O, NH or S(O)_(m) and wherein said alkynyl group is optionally independently substituted with one to two oxo groups, hydroxy, pyrroldinyl, pyrrolyl, tetrahydropyranyl, C₁₋₄ alkyl optionally substituted by one or more halogen atoms, nitrile, morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono- or di(C₁₋₃alkyl)amino optionally substituted by one or more halogen atoms; or silyl containing three C₁₋₄ alkyl groups optionally partially or fully halogenated; R₂ is independently: a C₁₋₅ branched or unbranched alkyl optionally partially or fully halogenated, acetyl, aroyl, C₁₋₄ branched or unbranched alkoxy, each being optionally partially or fully halogenated, halogen, methoxycarbonyl, C₁₋₂ alkyl-S(O)_(m) optionally partially or fully halogenated, or phenyl-S(O)_(m); C₁₋₃ alkoxy, hydroxy, nitrile, nitro, halogen; or amino-S(O)_(m)— wherein the N atom is optionally independently mono- or di-substituted by C₁₋₃alkyl or arylC₀₋₃alkyl, or amino wherein the N atom is optionally independently mono- or di-substituted by C₁₋₃alkyl, arylC₀₋₃alkyl, C₁₋₃acyl, C₁₋₄alkyl-S(O)_(m)— or arylC₀₋₃alkyl-S(O)_(m)—, each of the aforementioned alkyl and aryl in this subparagraph are optionally partially or fully halogenated and optionally substituted with one to two C₁₋₃ alkyl or C₁₋₃ alkoxy; R₃ is independently: phenyl, morpholino, pyridinyl, pyrimidinyl, pyrazinyl, pyrrolyl, pyrrolidinyl, imidazolyl, [1,3,4]oxadiazol, pyrazolyl, each is optionally substituted with one to three phenyl, naphthyl, heterocycle or heteroaryl as hereinabove described in this paragraph, C₁₋₆ alkyl which is optionally partially or fully halogenated, cyclopropanyl, cyclobutanyl, cyclopentanyl, cyclohexanyl, cycloheptanyl, bicyclopentanyl, bicyclohexanyl, bicycloheptanyl, phenyl C₁₋₅ alkyl, naphthyl C₁₋₅ alkyl, halogen, oxo, hydroxy, nitrile, C₁₋₃ alkoxy optionally partially or fully halogenated, phenyloxy, naphthyloxy, heteroaryloxy or heterocyclicoxy wherein the heteroaryl or heterocyclic moiety is as hereinabove described in this paragraph, nitro, amino, mono- or di-(C₁₋₃alkyl)amino, phenylamino, naphthylamino, heteroaryl or heterocyclic amino wherein the heteroaryl or heterocyclic moiety is as hereinabove described in this paragraph, NH₂C(O), a mono- or di-(C₁₋₃alkyl)aminocarbonyl, C₁₋₅ alkyl-C(O)—C₁₋₄ alkyl, mono- or di-(C₁₋₃alkyl)amino, mono- or di-(C₁₋₃)alkylamino-C₁₋₅ alkyl, mono- or di-(C₁₋₃alkyl)amino-S(O)₂, R₇—C₁₋₅ alkyl, R₈—C₁₋₅ alkoxy, R₉—C(O)—C₁₋₅ alkyl, R₁₀—C₁₋₅ alkyl(R₁₁)N, carboxy-mono- or di-(C₁₋₅)-alkyl-amino; C₁₋₃ alkyl or C₁₋₄ alkoxy each being optionally partially or fully halogenated or optionally substituted with R₁₇; OR₁₈ or C₁₋₆ alkyl optionally substituted with OR₁₈; amino or mono- or di-(C₁₋₅ alkyl)amino optionally substituted with R₁₉; R₂₀C(O)N(R₂₁)—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)—, R₂₃R₂₄NC(O)—C₁₋₂alkoxy or R₂₆C(O)CH₂N(R₂₁)—; C₂₋₄alkenyl substituted by R₂₃R₂₄NC(O)—; or C₂₋₄ alkynyl branched or unbranched carbon chain optionally partially or fully halogenated wherein one of the methylene groups is optionally replaced by O, and optionally independently substituted with one to two oxo groups, pyrroldinyl, pyrrolyl, morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl or one or more C₁₋₄ alkyl optionally substituted by one or more halogen atoms; C₁₋₃acyl; and R₂₃ and R₂₄ taken together optionally form imidazolyl, piperidinyl, morpholino, piperazinyl or a pyridinyl ring.
 4. The method according to claim 3 wherein: G is phenyl, pyridinyl, pyridonyl, naphthyl, quinolinyl, isoquinolinyl, pyrazinyl, 3,4-dihydro-2H-benzo[1,4]oxazinyl, benzothiophenyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, benzooxazolyl, indanyl, indolyl, indolinyl, indolonyl or indolinonyl, wherein G is optionally substituted by one or more R₁, R₂ or R₃; Ar is naphthyl; X is phenyl, imidazolyl, pyridinyl, pyrimidinyl, piperdinyl, piperazinyl, pyridazinyl or pyrazinyl each being optionally independently substituted with one to three C₁₋₄ alkyl, C₁₋₄alkoxy, hydroxy, nitrile, amino, mono- or di-(C₁₋₃ alkyl)amino, mono- or di-(C₁₋₃ alkylamino)carbonyl, NH₂C(O), C₁₋₆ alkyl-S(O)_(m) or halogen; Y is: a bond or a C₁₋₄ saturated carbon chain wherein one or more of the C atoms is optionally replaced by O, N or S and wherein Y is optionally independently substituted with nitrile or oxo; Z is: phenyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, imidazolyl, dihydrothiazolyl, dihydrothiazolyl sulfoxide, pyranyl, pyrrolidinyl, phenylpiperazinyl, tetrahydropyranyl, tetrahydrofuranyl, dioxolanyl, 2-oxa-5-aza-bicyclo[2.2.1]heptanyl, morpholino, thiomorpholino, thiomorpholino sulfoxidyl, piperidinyl, piperidinonyl, piperazinyl or tetrahydropyrimidonyl each of which are optionally substituted with one to two C₁₋₂ alkyl or C₁₋₂ alkoxy; or Z is hydroxy, C₁₋₃ alkyl, C₁₋₃ alkoxy, C₁₋₃ acylamino, C₁₋₃ alkylsulfonyl, nitrile C₁₋₃ alkyl or amino mono or di-substituted by C₁₋₃ alkoxyC₁₋₃ alkyl; each R₁ is independently: C₁₋₅ alkyl branched or unbranched optionally partially or fully halogenated, wherein one or more C atoms are optionally independently replaced by O, N or S(O)_(m), and wherein said C₁₋₅ alkyl is optionally substituted with oxo, dioxolanyl, pyrrolidinyl, furyl or phenyl each optionally substituted with one to three halogen, C₁₋₃ alkyl which is optionally partially or fully halogenated, hydroxy, nitrile and C₁₋₃alkoxy which is optionally partially or fully halogenated; cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, bicyclopentanyl or bicyclohexanyl, each being optionally partially or fully halogenated and optionally substituted with one to three C₁₋₃ alkyl groups optionally partially or fully halogenated, nitrile, hydroxyc₁₋₃alkyl or phenyl; and an analog of cyclopropyl, cyclobutyl, cyclopentanyl, cyclohexanyl, bicyclopentanyl or bicyclohexanyl wherein one ring methylene group is replaced by O; oxo; C₂₋₄ alkynyl optionally partially or fully halogenated wherein one or more methylene groups are optionally replaced by O, and optionally independently substituted with one to two oxo groups, hydroxy, pyrroldinyl, pyrrolyl, tetrahydropyranyl, C₁₋₄ alkyl optionally substituted by one or more halogen atoms, nitrile, morpholino, piperidinyl, piperazinyl, imidazolyl, phenyl, pyridinyl, tetrazolyl, or mono- or di(C₁₋₃ alkyl)amino optionally substituted by one or more halogen atoms; or silyl containing three C₁₋₂ alkyl groups optionally partially or fully halogenated; each R₂ is independently: a C₁₋₄ alkyl optionally partially or fully halogenated, C₁₋₄ alkoxy optionally partially or fully halogenated, bromo, chloro, fluoro, methoxycarbonyl, methyl-S(O)_(m), ethyl-S(O)_(m) each optionally partially or fully halogenated or phenyl-S(O)_(m); or R₂ is mono- or di-C₁₋₃ acylamino, amino-S(O)_(m) or S(O)_(m)amino wherein the N atom is mono- or di-substituted by C₁₋₃alkyl or phenyl, nitrile, nitro or amino; each R₃ is independently: phenyl, morpholino, pyridinyl, pyrimidinyl, pyrrolidinyl, 2,5-pyrrolidin-dionyl, imidazolyl, [1,3,4]oxadiazol, pyrazolyl, each of the aforementioned is optionally substituted with one to three C₁₋₃ alkyl which is optionally partially or fully halogenated, halogen, oxo, hydroxy, nitrile and C₁₋₃ alkoxy optionally partially or fully halogenated; C₁₋₃ alkyl or C₁₋₃ alkoxy optionally partially or fully halogenated or optionally substituted with R₁₇; OR₁₈ or C₁₋₃ alkyl optionally substituted with OR₁₈; amino or mono- or di-(C₁₋₃ alkyl)amino optionally substituted with R₁₉; R₂₀C(O)N(R₂₁)—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)—, NH₂C(O)methoxy or R₂₆C(O)CH₂N(R₂₁)—; C₂₋₄ alkenyl substituted by R₂₃R₂₄NC(O)—; or C₂₋₄ alkynyl substituted with pyrroldinyl or pyrrolyl; C₁₋₃acyl and R₂₃ and R₂₄ taken together optionally form morpholino.
 5. The method according to claim 4 wherein G is phenyl, pyridinyl, pyridonyl, 2-naphthyl, quinolinyl, isoquinolinyl, dihydrobenzofuranyl, indanyl, 5-indolyl, 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl, benzooxalolyl, 2,3-dihydrobenzooxazol-7-yl, 2-oxo-2,3-dihydro-1H-indol-5-yl, indolinyl, indolonyl, or indolinonyl, wherein G is optionally substituted by one or more R₁, R₂ or R₃; Ar is 1-naphthyl; X is: phenyl, imidazolyl, pyridinyl, pyrimidinyl, piperdinyl, piperazinyl, pyridazinyl or pyrazinyl; Y is: a bond or —CH₂—, —CH₂CH₂—, —C(O)—, —O—, —S—, —NH—CH₂CH₂CH₂—, —N(CH₃)—, CH₂(CN)CH₂—NH—CH₂ or —NH—; Z is morpholino, dioxolanyl, tetrahydrofuranyl, pyridinyl, 2-oxa-5-aza-bicyclo[2.2.1]heptanyl, C₁₋₃alkoxyphenylpiperazinyl, hydroxy, C₁₋₃alkyl, N,N-diC₁₋₃alkoxyC₁₋₃alkylamino, C₁₋₃acylamino, C₁₋₃alkylsulfonyl or nitrileC₁₋₃alkyl; each R₁ is independently: C₁₋₅ alkyl optionally partially or fully halogenated wherein one or more C atoms are optionally independently replaced by 0 or N, and wherein said C₁₋₅ alkyl is optionally substituted with oxo, dioxolanyl, pyrrolidinyl, furyl or phenyl optionally substituted by C₁₋₃alkoxy; cyclopropyl, cyclopentanyl, cyclohexanyl and bicyclopentanyl optionally substituted with one to three methyl groups optionally partially or fully halogenated, nitrile, hydroxymethyl or phenyl; or 2-tetrahydrofuranyl substituted by methyl; or trimethyl silyl; propynyl substituted hydroxy or tetrahydropyran-2-yloxy; R₂ is is mono- or di-C₁₋₃acylamino, amino-S(O)_(m) or S(O)_(m) amino wherein the N atom is mono- or di-substituted by C₁₋₃alkyl or phenyl, bromo, chloro, fluoro, nitrile, nitro, amino, methylsulfonyl optionally partially or fully halogenated or phenylsulfonyl; each R₃ is independently: phenyl, morpholino, pyridinyl, pyrimidinyl, pyrrolidinyl, 2,5-pyrrolidin-dionyl, imidazolyl, [1,3,4]oxadiazol or pyrazolyl, each is optionally substituted with C₁₋₂ alkyl which is optionally partially or fully halogenated; C₁₋₃ alkyl or C₁₋₃ alkoxy each being optionally partially or fully halogenated or optionally substituted with diethylamino; OR₁₈ or C₁₋₃ alkyl optionally substituted with OR₁₈; amino or mono- or di-(C₁₋₃ alkyl)amino optionally substituted with R₁₉; CH₃C(O)NH—, R₂₂O—; R₂₃R₂₄NC(O)—; R₂₆CH₂C(O)N(R₂₁)—, NH₂C(O)methoxy or R₂₆C(O)CH₂N(R₂₁)—; C₂₋₄alkenyl substituted by R₂₃R₂₄NC(O)—; or C₂₋₄ alkynyl substituted with pyrroldinyl or pyrrolyl; C₁₋₂acyl; and R₂₃ and R₂₄ are H or R₂₃ and R₂₄ taken together optionally form morpholino; and R₂₆ is morpholino.
 6. The method according to claim 5 wherein G is phenyl, pyridinyl, 5-indolyl, 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl, benzooxalolyl, 2,3-dihydrobenzooxazol-7-yl, 2-oxo-2,3-dihydro-1H-indol-5-yl or 2-naphthyl wherein G is optionally substituted by one or more R₁, R₂ or R₃; X is: imidazolyl, pyridinyl, pyrimidinyl or pyrazinyl; Y is: a bond, CH₂(CN)CH₂—NH—CH₂, —CH₂—, —NH—CH₂CH₂CH₂— or —NH—; Z is morpholin-4yl, dioxolan-2yl, tetrahydrofuranyl, pyridinyl, 2-oxa-5-aza-bicyclo[2.2.1]hept-5yl, methoxyphenylpiperazinyl, hydroxy, methyl, N,N-dimethoxyethylamino, acetylamino, methylsulfonyl or cyanoethyl; each R₁ is independently: tert-butyl, sec-butyl, tert-amyl, phenyl, tetrahydropyran-2-yloxypropynyl, hydroxypropynyl, trihalomethyl, 2,2-diethylpropionyl or cyclohexanyl; R₂ is chloro, nitro, amino, nitrile, methylsulfonylamino, diacetylamino, phenylsulfonylamino, N,N-di(methylsulfonyl)amino, methylsulfonyl or trihalomethylsulfonyl; R₃ is independently: methyl, C₁₋₃ alkoxy, methoxymethyl, hydroxypropyl, dimethylamino, C₁₋₄alkylamino, NH₂C(O)methoxy, acetyl, pyrrolidinyl, imidazolyl, pyrazolyl, morpholino or morpholinocarbonyl.
 7. The method according to claim 6 wherein X is pyridinyl.
 8. The method according to claim 7 wherein the pyridinyl is attached to Ar via the 3-pyridinyl position.
 9. A method of treating cancer, said method comprising administering to a patient a therapeutically effective amount of a compound chosen from: 1-(4-tert-Butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methyl-phenyl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; 1-(6-Chloro-4-trifluoromethyl-pyridin-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(4-Difluoromethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Methyl-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[2-Methoxy-5-(1-methyl-1-phenyl-ethyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; (5-tert-Butyl-2-methyl-phenyl)-carbamic acid 3-(5-{4-[3-(5-tert-butyl-2-methyl-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylamino)-propyl ester; 1-(6-tert-Butyl-benzo[1,3]dioxol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; 1,3-Bis-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-2-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2,3-Dimethyl-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(2-p-tolyloxy-5-trifluoromethyl-phenyl)-urea; 1-[2-(2-Methoxy-phenoxy)-5-trifluoromethyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-naphthalen-1-yl-urea; 1-{5-tert-Butyl-2-methyl-3-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-{5-tert-Butyl-2-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-Hydroxymethyl-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2-Methoxy-dibenzofuran-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2,5-Di-tert-butyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[3-(4-Bromo-1-methyl-1H-pyrazol-3-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Hydroxy-5,6,7,8-tetrahydro-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(1-Acetyl-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-oxazol-5-yl-phenyl)-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-[1,3,4]oxadiazol-2-yl-phenyl)-urea; 1-(2-Methoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; Furan-2-carboxylic acid (4-tert-butyl-2-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; 1-(2-Methoxy-4-phenylamino-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-Methoxy-2-methyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Hydroxy-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N,N-Diethyl-4-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzenesulfonamide; 1-(2,2-Difluoro-benzo[1,3]dioxol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-(1,1-Dimethyl-propyl)-2-phenoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-(2,2-Dimethyl-propionyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 2-Chloro-5-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzoic acid isopropyl ester; 1-(4-Amino-3,5-dibromo-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(3-hydroxy-prop-1-ynyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-2-(3-hydroxy-prop-1-ynyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butoxy-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-(1-Cyano-cyclopropyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2-diethylamino-ethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-[1,3]dioxolan-2-yl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-pyrrolidin-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-dimethylamino-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-propoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-hydroxymethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 2-(5-tert-Butyl-2-methoxy-phenyl)-N-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-acetamide; 1-(2-Methoxy-5-phenoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-cyclopentyloxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-pyridin-3-yl-pyrrolidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-Cyclohexyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2,4-Dimethoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(6-tert-Butyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-methyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-Acetyl-N-(5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; 1-(6-tert-Butyl-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[6-tert-Butyl-4-(2-morpholin-4-yl-ethyl)-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-isopropoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-imidazol-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-4-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide; 1-(5-tert-Butyl-3-ethylamino-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-bis(methanesulfon)amide; 1-[5-tert-Butyl-2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2-Methanesulfinyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2-Ethanesulfonyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-{[Bis-(2-methoxy-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-dimethylamino-pyrrolidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; N-[1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-pyrrolidin-3-yl]-acetamide; 1-(1-Acetyl-3,3-dimethyl-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-propionamide; 1-(5-tert-Butyl-2-methyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethanesulfonyl-phenyl)-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-isobutyramide; 2-(4-tert-Butyl-2-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenoxy)-acetamide; 1-(5-tert-Butyl-2-oxo-2,3-dihydro-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(6-tert-Butyl-3-cyano-2-methoxymethoxy-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(6-tert-Butyl-3-cyano-2-hydroxy-pyridin-4-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-3-cyano-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(1,3,3-trimethyl-2,3-dihydro-1H-indol-5-yl)-urea; 1-(5-tert-Butyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-benzenesulfonamide; Ethanesulfonic acid (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-3-[4-(4-morpholin-4-ylmethyl-piperidin-1-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 2,2,2-Trifluoro-ethanesulfonic acid (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; N-(5-{4-[3-(5-tert-Butyl-2-methyl-phenyl)-ureido]-naphthalen-1-yl}-pyrazin-2-yl)-methanesulfonamide; 1-[4-(6-{[Bis-(2-cyano-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-methyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-piperidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-tetrahydro-thiopyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(tetrahydro-pyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-(tetrahydro-furan-2-ylmethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methoxymethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-morpholin-4-yl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methyl-3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperidine-3-carboxylic acid amide; 1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperidine-4-carboxylic acid amide; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-114-thiomorpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-{4-[6-(4-Acetyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-3-(5-tert-butyl-2-methoxy-phenyl)-urea; 4-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperazine-1-carboxylic acid ethyl ester; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-pyridin-3-yl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(tetrahydro-furan-3-ylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-pyridin-3-ylmethyl-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-methylsulfanyl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-oxa-5-aza-bicyclo[2.2.1]hept-5-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(2-piperazin-1-yl-ethylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-pyrimidin-2-yl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-pyridin-2-yl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[4-(3-methoxy-phenyl)-piperazin-1-ylmethyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(morpholine-4-carbonyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-thia-5-aza-bicyclo[2.2.1]hept-5-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(5-morpholin-4-ylmethyl-pyrazin-2-yl)-naphthalen-1-yl]-urea; 1-(6-tert-Butyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-yl)-acetamide; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-N-methyl-acetamide; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-2,2,2-trifluoro-acetamide; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(pyridin-3-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(pyridin-3-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; [4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-carbamic acid 3-tert-butyl-phenyl ester and N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide or the pharmaceutically acceptable salts thereof.
 10. A method of treating cancer, said method comprising administering to a patient a therapeutically effective amount of a compound chosen from: 1-(3-Methyl-naphthalen-2-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; 1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2,3-Dimethyl-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-{5-tert-Butyl-2-methyl-3-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-phenyl}-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2-Methoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-(2,2-Dimethyl-propionyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(3-hydroxy-prop-1-ynyl)-2-methyl-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-2-(3-hydroxy-prop-1-ynyl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butoxy-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-(1-Cyano-cyclopropyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[5-tert-Butyl-3-(2-diethylamino-ethyl)-2-methoxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-[1,3]dioxolan-2-yl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-pyrrolidin-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-dimethylamino-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-propoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-hydroxymethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-Cyclohexyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2,4-Dimethoxy-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-3-nitro-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-methyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-Acetyl-N-(5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-acetamide; 1-(6-tert-Butyl-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-ethoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-isopropoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-imidazol-1-yl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-3-ethylamino-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-bis(methanesulfon)amide; 1-[5-tert-Butyl-2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(2-Methanesulfinyl-5-trifluoromethyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-{[Bis-(2-methoxy-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; N-[1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-pyrrolidin-3-yl]-acetamide; 1-(1-Acetyl-3,3-dimethyl-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-propionamide; 1-(5-tert-Butyl-2-methyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-3-(3-trifluoromethanesulfonyl-phenyl)-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-isobutyramide; 2-(4-tert-Butyl-2-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenoxy)-acetamide; 1-(5-tert-Butyl-2-oxo-2,3-dihydro-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-3-cyano-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-benzooxazol-7-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-benzenesulfonamide; Ethanesulfonic acid (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(2-morpholin-4-ylmethyl-pyrimidin-5-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methylsulfanyl-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 2,2,2-Trifluoro-ethanesulfonic acid (5-tert-butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-amide; N-(5-{4-[3-(5-tert-Butyl-2-methyl-phenyl)-ureido]-naphthalen-1-yl}-pyrazin-2-yl)-methanesulfonamide; 1-[4-(6-{[Bis-(2-cyano-ethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-3-(5-tert-butyl-2-methoxy-phenyl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(4-methyl-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-thiomorpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-piperidin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-tetrahydro-thiopyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(tetrahydro-pyran-4-ylamino)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-(tetrahydro-furan-2-ylmethyl)-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methoxymethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-methyl-3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-ylmethyl)-piperidine-3-carboxylic acid amide; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(1-oxo-114-thiomorpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(3-oxo-piperazin-1-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[(tetrahydro-furan-3-ylamino)-methyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(6-{[(2-cyano-ethyl)-pyridin-3-ylmethyl-amino]-methyl}-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2-oxa-5-aza-bicyclo[2.2.1]hept-5-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(2,6-dimethyl-morpholin-4-ylmethyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-(4-{6-[4-(3-methoxy-phenyl)-piperazin-1-ylmethyl]-pyridin-3-yl}-naphthalen-1-yl)-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(morpholine-4-carbonyl)-pyridin-3-yl]-naphthalen-1-yl}-urea; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-[4-(5-morpholin-4-ylmethyl-pyrazin-2-yl)-naphthalen-1-yl]-urea; 1-(6-tert-Butyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-{4-[3-(5-tert-Butyl-2-methoxy-phenyl)-ureido]-naphthalen-1-yl}-pyridin-2-yl)-acetamide; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-N-methyl-acetamide; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-2,2,2-trifluoro-acetamide; 1-(5-tert-Butyl-2-methoxy-phenyl)-3-{4-[6-(pyridin-3-yloxy)-pyridin-3-yl]-naphthalen-1-yl}-urea; [4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-carbamic acid 3-tert-butyl-phenyl ester and N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide and or the pharmaceutically salts thereof.
 11. A method of treating cancer, said method comprising administering to a patient a therapeutically effective amount of a compound chosen from: 1-(5-tert-Butyl-2-methylsulfanyl-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-chloro-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; 1-(5-tert-Butyl-2-methylamino-pyridin-3-yl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea; N-(5-tert-Butyl-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-2-oxo-2H-pyridin-1-yl)-methanesulfonamide; 5-tert-Butyl-7-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzooxazole-2-carboxylic acid amide; 2-(5-tert-Butyl-7-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzooxazol-2-yl)-acetamide; 5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-benzamide; N-(5-tert-Butyl-2-methoxy-3-{3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-ureido}-phenyl)-methanesulfonamide; 1-(3-Amino-5-tert-butyl-2-methoxy-phenyl)-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea and 1-[5-tert-Butyl-3-(2,3-dihydroxy-propyl)-2-hydroxy-phenyl]-3-[4-(6-morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-urea or the pharmaceutically acceptable salts thereof.
 12. The method according to claims 1, 9, 10 or 11 wherein the cancer is chosen from cancer cachexia, multiple myeloma, acute myelogenous leukemia and Castleman's disease.
 13. The method according to claims 1, 9, 10 or 11 wherein the method involves inhibiting proliferation of acute myelogenous leukemia blasts.
 14. The method according to claims 1, 9, 10 or 11 wherein the cancer is a plasma cell dyscrasias.
 15. The method according to claim 1, 9, 10 or 11 wherein treament is done in conjunction with genotoxic therapy.
 16. The method according to claim 1, 9, 10 or 11 wherein the method involves treating tumor cells. 